A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv967067



Internal ID16261023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:82857249..82990126hg38UCSC Ensembl
Innerchr3:82906400..83039277hg19UCSC Ensembl
Innerchr3:82989090..83121967hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38132878
hg19132878
hg18132878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590805
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv967067
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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