A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016124



Internal ID19105342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78147537..78329517hg38UCSC Ensembl
Innerchr6:78857254..79039234hg19UCSC Ensembl
Innerchr6:78913973..79095953hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38181981
hg19181981
hg18181981
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6024n100
Supporting Variantsnssv3659063, nssv3659062
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)nsv1016124
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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