A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522764



Internal ID15450057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5486573..5527407hg38UCSC Ensembl
InnerchrX:5404614..5445448hg19UCSC Ensembl
InnerchrX:5414614..5455448hg18UCSC Ensembl
InnerchrX:5264350..5305184hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3840835
hg1940835
hg1840835
hg1740835
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698404
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522764
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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