A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016925



Internal ID18759460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:131097392..131131160hg38UCSC Ensembl
Innerchr6:131418532..131452300hg19UCSC Ensembl
Innerchr6:131460225..131493993hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3833769
hg1933769
hg1833769
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6146n100
Supporting Variantsnssv3654392, nssv3654393
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)nsv1016925
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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