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nsv5535698

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:50

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 92 SVs from 18 studies. See in: genome view    
Submitted genomic87,332,725-87,332,774Question Mark
Overlapping variant regions from other studies: 92 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):88,042,443-88,042,492Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5535698Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr687,332,72587,332,774
nsv5535698RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr688,042,44388,042,492

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16984981insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16984981Submitted genomicNC_000006.12:g.873
32725_87332774ins8
6
GRCh38 (hg38)NC_000006.12Chr687,332,72587,332,774
nssv16984981RemappedPerfectNC_000006.11:g.880
42443_88042492ins8
6
GRCh37.p13First PassNC_000006.11Chr688,042,44388,042,492

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)
nssv169849810.51532996404
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