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nsv5556816

  • 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: 90 SVs from 22 studies. See in: genome view    
Submitted genomic65,049,920-65,049,971Question Mark
Overlapping variant regions from other studies: 90 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):65,516,638-65,516,689Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5556816Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1465,049,92065,049,971
nsv5556816RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1465,516,63865,516,689

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17696759sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17696759Submitted genomicNC_000014.9:g.6504
9920_65049971ins12
10
GRCh38 (hg38)NC_000014.9Chr1465,049,92065,049,971
nssv17696759RemappedPerfectNC_000014.8:g.6551
6638_65516689ins12
10
GRCh37.p13First PassNC_000014.8Chr1465,516,63865,516,689

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)
nssv17696759<0.00116404
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