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nsv5414032

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:788

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 117 SVs from 21 studies. See in: genome view    
Submitted genomic153,975,905-153,976,692Question Mark
Overlapping variant regions from other studies: 128 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):153,948,381-153,949,168Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5414032Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1153,975,905153,976,692
nsv5414032RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1153,948,381153,949,168

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16890644deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16890644Submitted genomicNC_000001.11:g.153
975905_153976692de
l
GRCh38 (hg38)NC_000001.11Chr1153,975,905153,976,692
nssv16890644RemappedPerfectNC_000001.10:g.153
948381_153949168de
l
GRCh37.p13First PassNC_000001.10Chr1153,948,381153,949,168

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16890644<0.00116404
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