A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518844



Internal ID15446137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:36031748..36066715hg38UCSC Ensembl
Innerchr1:36497349..36532316hg19UCSC Ensembl
Innerchr1:36269936..36304903hg18UCSC Ensembl
Innerchr1:36166442..36201409hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3834968
hg1934968
hg1834968
hg1734968
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694280
Samples
Known GenesAGO3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518844
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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