A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522437



Internal ID15103044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:24754031..24860225hg38UCSC Ensembl
Innerchr1:25080522..25186716hg19UCSC Ensembl
Innerchr1:24953109..25059303hg18UCSC Ensembl
Innerchr1:24825828..24932022hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38106195
hg19106195
hg18106195
hg17106195
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705795
Samples
Known GenesCLIC4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522437
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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