A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035096



Internal ID19124315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63555706..63722096hg38UCSC Ensembl
Innerchr9:68151440..68317830hg19UCSC Ensembl
Innerchr9:67641260..67807650hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38166391
hg19166391
hg18166391
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7635n100
Supporting Variantsnssv3694818
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)nsv1035096
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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