A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962143



Internal ID16256099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36054449..36226037hg38UCSC Ensembl
Innerchr3:36095941..36267529hg19UCSC Ensembl
Innerchr3:36070945..36242533hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38171589
hg19171589
hg18171589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590064
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)nssv962143
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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