A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032022



Internal ID19121244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78147537..78331916hg38UCSC Ensembl
Innerchr6:78857254..79041633hg19UCSC Ensembl
Innerchr6:78913973..79098352hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38184380
hg19184380
hg18184380
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6024n100
Supporting Variantsnssv3659064
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)nsv1032022
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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