A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6016n100



Internal ID22792103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74655132..74713171hg38UCSC Ensembl
chr6:75364848..75422887hg19UCSC Ensembl
chr6:75421568..75479607hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3858040
hg1958040
hg1858040
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027029, nsv1015675
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)dgv6016n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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