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nsv5528258

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,524

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 129 SVs from 21 studies. See in: genome view    
Submitted genomic39,409,499-39,412,022Question Mark
Overlapping variant regions from other studies: 129 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):39,900,139-39,902,662Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5528258Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1939,409,49939,412,022
nsv5528258RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1939,900,13939,902,662

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723334deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723334Submitted genomicNC_000019.10:g.394
09499_39412022del
GRCh38 (hg38)NC_000019.10Chr1939,409,49939,412,022
nssv17723334RemappedPerfectNC_000019.9:g.3990
0139_39902662del
GRCh37.p13First PassNC_000019.9Chr1939,900,13939,902,662

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)
nssv17723334<0.00116404
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