A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3694819



Internal ID18993100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63555706..63763076hg38UCSC Ensembl
Innerchr9:68151440..68358810hg19UCSC Ensembl
Innerchr9:67641260..67848630hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38207371
hg19207371
hg18207371
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020821
Supporting Variants
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)nssv3694819
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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