A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6119n100



Internal ID22792206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:103269703..103314174hg38UCSC Ensembl
chr6:103717578..103762049hg19UCSC Ensembl
chr6:103824271..103868742hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3844472
hg1944472
hg1844472
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1023620, nsv1031596, nsv1018096, nsv1026904
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)dgv6119n100
Frequency
Sample Size11257
Observed Gain29
Observed Loss18
Observed Complex0
Frequencyn/a


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