A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687423



Internal ID15424075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:116807112..116869846hg38UCSC Ensembl
InnerchrX:115941080..116003814hg19UCSC Ensembl
InnerchrX:115825108..115887842hg18UCSC Ensembl
InnerchrX:115722962..115785696hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3862735
hg1962735
hg1862735
hg1762735
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516826
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687423
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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