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nsv5482329

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:54

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1015 SVs from 76 studies. See in: genome view    
Submitted genomic39,385,802-39,385,855Question Mark
Overlapping variant regions from other studies: 1015 SVs from 76 studies. See in: genome view    
Remapped(Score: Perfect):39,243,321-39,243,374Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5482329Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr839,385,80239,385,855
nsv5482329RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr839,243,32139,243,374

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17009597deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17009597Submitted genomicNC_000008.11:g.393
85802_39385855del
GRCh38 (hg38)NC_000008.11Chr839,385,80239,385,855
nssv17009597RemappedPerfectNC_000008.10:g.392
43321_39243374del
GRCh37.p13First PassNC_000008.10Chr839,243,32139,243,374

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)
nssv17009597<0.00126404
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