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esv33845

  • Variant Calls:3
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:45,719

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 828 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):97,712,227-97,757,945Question Mark
Overlapping variant regions from other studies: 828 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):97,047,931-97,093,649Question Mark
Overlapping variant regions from other studies: 108 SVs from 10 studies. See in: genome view    
Submitted genomic97,073,687-97,119,405Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv33845RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr597,712,22797,757,945
esv33845RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr597,047,93197,093,649
esv33845Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000005.8Chr597,073,68797,119,405

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv101650copy number loss21909Oligo aCGHProbe signal intensity171
essv93571copy number loss22128Oligo aCGHProbe signal intensity178
essv98230copy number loss21772Oligo aCGHProbe signal intensity211

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv101650RemappedPerfectNC_000005.10:g.(97
696103_97712227)_(
97757945_97765487)
del		GRCh38.p12First PassNC_000005.10Chr597,696,10397,712,22797,757,94597,765,487
essv93571RemappedPerfectNC_000005.10:g.(97
696103_97712227)_(
97757945_97765487)
del		GRCh38.p12First PassNC_000005.10Chr597,696,10397,712,22797,757,94597,765,487
essv98230RemappedPerfectNC_000005.10:g.(97
696103_97712227)_(
97757945_97765487)
del		GRCh38.p12First PassNC_000005.10Chr597,696,10397,712,22797,757,94597,765,487
essv101650RemappedPerfectNC_000005.9:g.(970
31807_97047931)_(9
7093649_97101191)d
el		GRCh37.p13First PassNC_000005.9Chr597,031,80797,047,93197,093,64997,101,191
essv93571RemappedPerfectNC_000005.9:g.(970
31807_97047931)_(9
7093649_97101191)d
el		GRCh37.p13First PassNC_000005.9Chr597,031,80797,047,93197,093,64997,101,191
essv98230RemappedPerfectNC_000005.9:g.(970
31807_97047931)_(9
7093649_97101191)d
el		GRCh37.p13First PassNC_000005.9Chr597,031,80797,047,93197,093,64997,101,191
essv101650Submitted genomicNC_000005.8:g.(970
57563_97073687)_(9
7119405_97126947)d
el		NCBI35 (hg17)NC_000005.8Chr597,057,56397,073,68797,119,40597,126,947
essv93571Submitted genomicNC_000005.8:g.(970
57563_97073687)_(9
7119405_97126947)d
el		NCBI35 (hg17)NC_000005.8Chr597,057,56397,073,68797,119,40597,126,947
essv98230Submitted genomicNC_000005.8:g.(970
57563_97073687)_(9
7119405_97126947)d
el		NCBI35 (hg17)NC_000005.8Chr597,057,56397,073,68797,119,40597,126,947

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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