A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522787



Internal ID15450080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:93014428..93533554hg38UCSC Ensembl
InnerchrX:92269427..92788553hg19UCSC Ensembl
InnerchrX:92156083..92675209hg18UCSC Ensembl
InnerchrX:92075572..92594698hg17UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg38519127
hg19519127
hg18519127
hg17519127
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698431
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522787
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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