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nsv5427233

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,889

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 242 SVs from 27 studies. See in: genome view    
Submitted genomic65,685,501-65,702,389Question Mark
Overlapping variant regions from other studies: 242 SVs from 27 studies. See in: genome view    
Remapped(Score: Good):64,905,362-64,922,251Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5427233Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX65,685,50165,702,389
nsv5427233RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX64,905,36264,922,251

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17740406duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17740406Submitted genomicNC_000023.11:g.656
85501_65702389dup
GRCh38 (hg38)NC_000023.11ChrX65,685,50165,702,389
nssv17740406RemappedGoodNC_000023.10:g.649
05362_64922251dup
GRCh37.p13First PassNC_000023.10ChrX64,905,36264,922,251

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)
nssv177404060.004184798
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