A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701720



Internal ID15438372
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525581
Supporting Variants
Samples
Known GenesDAB1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701720
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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