A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020821



Internal ID19110039
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 StatusM
Merged Variantsdgv7635n100
Supporting Variantsnssv3694819
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)nsv1020821
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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