A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525307



Internal ID15452600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:42989395..43020480hg38UCSC Ensembl
Innerchr2:43216535..43247619hg19UCSC Ensembl
Innerchr2:43070039..43101123hg18UCSC Ensembl
Innerchr2:43128186..43159270hg17UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3831086
hg1931085
hg1831085
hg1731085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701414
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525307
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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