A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694133



Internal ID15430785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:121408071..121567008hg38UCSC Ensembl
InnerchrX:120541925..120700862hg19UCSC Ensembl
InnerchrX:120369606..120528543hg18UCSC Ensembl
InnerchrX:120267460..120426397hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38158938
hg19158938
hg18158938
hg17158938
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522118
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694133
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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