A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524772



Internal ID15452065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:24931117..24937874hg38UCSC Ensembl
Innerchr2:25153986..25160743hg19UCSC Ensembl
Innerchr2:25007490..25014247hg18UCSC Ensembl
Innerchr2:25065637..25072394hg17UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg386758
hg196758
hg186758
hg176758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700763
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524772
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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