A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv986700



Internal ID16280656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195054607..195066805hg38UCSC Ensembl
Innerchr3:194775336..194787534hg19UCSC Ensembl
Innerchr3:196256625..196268823hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3812199
hg1912199
hg1812199
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592968
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)nssv986700
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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