A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6142n100



Internal ID20157758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121615257..121705135hg38UCSC Ensembl
chr6:121936403..122026281hg19UCSC Ensembl
chr6:121978102..122067980hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3889879
hg1989879
hg1889879
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018836, nsv1031933
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)dgv6142n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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