A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525581



Internal ID15452874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:58117307..58132554hg38UCSC Ensembl
Innerchr1:58582979..58598226hg19UCSC Ensembl
Innerchr1:58355567..58370814hg18UCSC Ensembl
Innerchr1:58295000..58310247hg17UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3815248
hg1915248
hg1815248
hg1715248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701720
Samples
Known GenesDAB1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525581
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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