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nsv5416491

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32,637,437

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 40789 SVs from 105 studies. See in: genome view    
Submitted genomic39,941,083-72,578,519Question Mark
Overlapping variant regions from other studies: 40332 SVs from 105 studies. See in: genome view    
Remapped(Score: Good):39,800,337-71,530,833Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5416491Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX39,941,08372,578,519
nsv5416491RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX39,800,33771,530,833

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17736488deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17736488Submitted genomicNC_000023.11:g.399
41083_72578519del
GRCh38 (hg38)NC_000023.11ChrX39,941,08372,578,519
nssv17736488RemappedGoodNC_000023.10:g.398
00337_71530833del
GRCh37.p13First PassNC_000023.10ChrX39,800,33771,530,833

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)
nssv177364880.002114805
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