A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024073



Internal ID19113290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78147537..78336932hg38UCSC Ensembl
Innerchr6:78857254..79046649hg19UCSC Ensembl
Innerchr6:78913973..79103368hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38189396
hg19189396
hg18189396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6024n100
Supporting Variantsnssv3659075, nssv3659073, nssv3659074
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)nsv1024073
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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