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nsv5561529

  • 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: 65 SVs from 15 studies. See in: genome view    
Submitted genomic157,498,816-157,498,867Question Mark
Overlapping variant regions from other studies: 65 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):156,925,824-156,925,875Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5561529Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5157,498,816157,498,867
nsv5561529RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5156,925,824156,925,875

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16975951line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16975951Submitted genomicNC_000005.10:g.157
498816_157498867in
s6018
GRCh38 (hg38)NC_000005.10Chr5157,498,816157,498,867
nssv16975951RemappedPerfectNC_000005.9:g.1569
25824_156925875ins
6018
GRCh37.p13First PassNC_000005.9Chr5156,925,824156,925,875

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)
nssv16975951<0.00116404
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