A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524638



Internal ID15105245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:143230549..143238941hg38UCSC Ensembl
Innerchr2:143988118..143996510hg19UCSC Ensembl
Innerchr2:143704588..143712980hg18UCSC Ensembl
Innerchr2:143821850..143830242hg17UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg388393
hg198393
hg188393
hg178393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700603
Samples
Known GenesARHGAP15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524638
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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