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nsv5555868

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 67 SVs from 15 studies. See in: genome view    
Submitted genomic69,307,759-69,307,810Question Mark
Overlapping variant regions from other studies: 67 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):69,774,476-69,774,527Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5555868Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1469,307,75969,307,810
nsv5555868RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1469,774,47669,774,527

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17697827sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17697827Submitted genomicNC_000014.9:g.6930
7759_69307810ins46
5
GRCh38 (hg38)NC_000014.9Chr1469,307,75969,307,810
nssv17697827RemappedPerfectNC_000014.8:g.6977
4476_69774527ins46
5
GRCh37.p13First PassNC_000014.8Chr1469,774,47669,774,527

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)
nssv17697827<0.00116404
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