A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv960942



Internal ID16254898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:30058593..30122198hg38UCSC Ensembl
Innerchr3:30100084..30163689hg19UCSC Ensembl
Innerchr3:30075088..30138693hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3863606
hg1963606
hg1863606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590027
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)nssv960942
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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