A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963557



Internal ID15910827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62724769..62729200hg38UCSC Ensembl
Innerchr3:62710444..62714875hg19UCSC Ensembl
Innerchr3:62685484..62689915hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg384432
hg194432
hg184432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590445
Supporting Variants
Samples
Known GenesCADPS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv963557
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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