A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv965556



Internal ID15912826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:71754058..71754987hg38UCSC Ensembl
Innerchr3:71803209..71804138hg19UCSC Ensembl
Innerchr3:71885899..71886828hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38930
hg19930
hg18930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590611
Supporting Variants
Samples
Known GenesEIF4E3, GPR27
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv965556
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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