A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv985747



Internal ID15933017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:194339977..194341836hg38UCSC Ensembl
Innerchr3:194060706..194062565hg19UCSC Ensembl
Innerchr3:195542401..195544260hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381860
hg191860
hg181860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592957
Supporting Variants
Samples
Known GenesCPN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv985747
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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