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nsv6623433

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,786

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 140 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):26,814,620-26,833,405Question Mark
Overlapping variant regions from other studies: 140 SVs from 31 studies. See in: genome view    
Submitted genomic26,825,941-26,844,726Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv6623433RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1626,814,62026,833,405
nsv6623433Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000016.9Chr1626,825,94126,844,726

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv18283975duplicationOSC2401SNP arrayProbe signal intensity8

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv18283975RemappedPerfectNC_000016.10:g.(?_
26814620)_(2683340
5_?)dup
GRCh38.p12First PassNC_000016.10Chr1626,814,62026,833,405
nssv18283975Submitted genomicNC_000016.9:g.(?_2
6825941)_(26844726
_?)dup
GRCh37 (hg19)NC_000016.9Chr1626,825,94126,844,726

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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