A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962390



Internal ID16256346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41052084..41082244hg38UCSC Ensembl
Innerchr3:41093575..41123735hg19UCSC Ensembl
Innerchr3:41068579..41098739hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3830161
hg1930161
hg1830161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590114
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)nssv962390
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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