A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525804



Internal ID15106411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:77188498..77202141hg38UCSC Ensembl
Innerchr3:77237649..77251292hg19UCSC Ensembl
Innerchr3:77320339..77333982hg18UCSC Ensembl
Innerchr3:77320339..77333982hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3813644
hg1913644
hg1813644
hg1713644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701988
Samples
Known GenesROBO2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525804
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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