A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6118n100



Internal ID22792205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:103265324..103323057hg38UCSC Ensembl
chr6:103713199..103770932hg19UCSC Ensembl
chr6:103819892..103877625hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3857734
hg1957734
hg1857734
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033482, nsv1015838, nsv1020685, nsv1016866, nsv1025776, nsv1020303, nsv1018385, nsv1024578
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)dgv6118n100
Frequency
Sample Size11257
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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