A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046431



Internal ID19135650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77155482..77171214hg38UCSC Ensembl
Innerchr9:79770398..79786130hg19UCSC Ensembl
Innerchr9:78960218..78975950hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3815733
hg1915733
hg1815733
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7683n100
Supporting Variantsnssv3696378
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046431
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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