A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039876



Internal ID19129095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77155482..77171645hg38UCSC Ensembl
Innerchr9:79770398..79786561hg19UCSC Ensembl
Innerchr9:78960218..78976381hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3816164
hg1916164
hg1816164
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7683n100
Supporting Variantsnssv3696385, nssv3696384
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)nsv1039876
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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