A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152465



Internal ID15533856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4656425..4751836hg38UCSC Ensembl
Innerchr3:4698109..4793520hg19UCSC Ensembl
Innerchr3:4673109..4768520hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3895412
hg1995412
hg1895412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589454
Supporting Variants
SamplesNINDS_223
Known GenesEGOT, ITPR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152465
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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