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nsv5422645

  • 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: 98 SVs from 21 studies. See in: genome view    
Submitted genomic76,766,067-76,766,118Question Mark
Overlapping variant regions from other studies: 98 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):77,232,410-77,232,461Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5422645Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1476,766,06776,766,118
nsv5422645RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1477,232,41077,232,461

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17697977alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17697977Submitted genomicNC_000014.9:g.7676
6067_76766118ins27
0
GRCh38 (hg38)NC_000014.9Chr1476,766,06776,766,118
nssv17697977RemappedPerfectNC_000014.8:g.7723
2410_77232461ins27
0
GRCh37.p13First PassNC_000014.8Chr1477,232,41077,232,461

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)
nssv17697977<0.00116404
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