A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151912



Internal ID15881200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65192321..65226921hg38UCSC Ensembl
Innerchr3:65177996..65212596hg19UCSC Ensembl
Innerchr3:65153036..65187636hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3834601
hg1934601
hg1834601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590477
Supporting Variants
SamplesNINDS_83
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151912
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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