nsv5524198

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:480

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 121 SVs from 20 studies. See in: genome view    
Submitted genomic35,825,948-35,826,427Question Mark
Overlapping variant regions from other studies: 121 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):36,316,850-36,317,329Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5524198Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1935,825,94835,826,427
nsv5524198RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,316,85036,317,329

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723046deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723046Submitted genomicNC_000019.10:g.358
25948_35826427del
GRCh38 (hg38)NC_000019.10Chr1935,825,94835,826,427
nssv17723046RemappedPerfectNC_000019.9:g.3631
6850_36317329del
GRCh37.p13First PassNC_000019.9Chr1936,316,85036,317,329

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)
nssv17723046<0.00126404
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