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nsv5528649

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,142

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 148 SVs from 24 studies. See in: genome view    
Submitted genomic39,241,418-39,244,559Question Mark
Overlapping variant regions from other studies: 148 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):39,732,058-39,735,199Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5528649Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1939,241,41839,244,559
nsv5528649RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1939,732,05839,735,199

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723327deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723327Submitted genomicNC_000019.10:g.392
41418_39244559del
GRCh38 (hg38)NC_000019.10Chr1939,241,41839,244,559
nssv17723327RemappedPerfectNC_000019.9:g.3973
2058_39735199del
GRCh37.p13First PassNC_000019.9Chr1939,732,05839,735,199

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)
nssv17723327<0.00116404
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