A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv968103



Internal ID16262059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:96813227..96814420hg38UCSC Ensembl
Innerchr3:96532071..96533264hg19UCSC Ensembl
Innerchr3:98014761..98015954hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg381194
hg191194
hg181194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591038
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)nssv968103
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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