A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525739



Internal ID15453032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:98578777..98683088hg38UCSC Ensembl
InnerchrX:97833775..97938086hg19UCSC Ensembl
InnerchrX:97720431..97824742hg18UCSC Ensembl
InnerchrX:97639920..97744231hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38104312
hg19104312
hg18104312
hg17104312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701904
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525739
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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