A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051349



Internal ID19140568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77155482..77171918hg38UCSC Ensembl
Innerchr9:79770398..79786834hg19UCSC Ensembl
Innerchr9:78960218..78976654hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3816437
hg1916437
hg1816437
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7683n100
Supporting Variantsnssv3696386
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)nsv1051349
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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