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nsv5426889

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,714

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 285 SVs from 36 studies. See in: genome view    
Submitted genomic73,599,175-73,611,888Question Mark
Overlapping variant regions from other studies: 285 SVs from 36 studies. See in: genome view    
Remapped(Score: Good):72,819,011-72,831,723Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5426889Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX73,599,17573,611,888
nsv5426889RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX72,819,01172,831,723

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17740727deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17740727Submitted genomicNC_000023.11:g.735
99175_73611888del
GRCh38 (hg38)NC_000023.11ChrX73,599,17573,611,888
nssv17740727RemappedGoodNC_000023.10:g.728
19011_72831723del
GRCh37.p13First PassNC_000023.10ChrX72,819,01172,831,723

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)
nssv177407270.0622974803
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