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nsv5408619

  • 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: 138 SVs from 41 studies. See in: genome view    
Submitted genomic66,636,845-66,636,896Question Mark
Overlapping variant regions from other studies: 138 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):66,101,832-66,101,883Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5408619Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr766,636,84566,636,896
nsv5408619RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr766,101,83266,101,883

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16997224alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16997224Submitted genomicNC_000007.14:g.666
36845_66636896ins2
80
GRCh38 (hg38)NC_000007.14Chr766,636,84566,636,896
nssv16997224RemappedPerfectNC_000007.13:g.661
01832_66101883ins2
80
GRCh37.p13First PassNC_000007.13Chr766,101,83266,101,883

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)
nssv16997224<0.00116404
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