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nsv5530435

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,104

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 161 SVs from 16 studies. See in: genome view    
Submitted genomic46,559,409-46,561,512Question Mark
Overlapping variant regions from other studies: 161 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):44,139,372-44,141,475Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5530435Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1846,559,40946,561,512
nsv5530435RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1844,139,37244,141,475

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17717907deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17717907Submitted genomicNC_000018.10:g.465
59409_46561512del
GRCh38 (hg38)NC_000018.10Chr1846,559,40946,561,512
nssv17717907RemappedPerfectNC_000018.9:g.4413
9372_44141475del
GRCh37.p13First PassNC_000018.9Chr1844,139,37244,141,475

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)
nssv17717907<0.00116404
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