A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702359



Internal ID15439011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5341074..5350397hg38UCSC Ensembl
InnerchrX:5259115..5268438hg19UCSC Ensembl
InnerchrX:5269115..5278438hg18UCSC Ensembl
InnerchrX:5118851..5128174hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg389324
hg199324
hg189324
hg179324
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526111
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702359
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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