A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962986



Internal ID15910256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:47449685..47451848hg38UCSC Ensembl
Innerchr3:47491175..47493338hg19UCSC Ensembl
Innerchr3:47466179..47468342hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382164
hg192164
hg182164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590230
Supporting Variants
Samples
Known GenesSCAP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv962986
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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