A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524562



Internal ID15451855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:10095408..10098028hg38UCSC Ensembl
InnerchrX:10063448..10066068hg19UCSC Ensembl
InnerchrX:10023448..10026068hg18UCSC Ensembl
InnerchrX:9873184..9875804hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg382621
hg192621
hg182621
hg172621
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700516
Samples
Known GenesWWC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524562
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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