A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6116n100



Internal ID22792203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:102993108..103072748hg38UCSC Ensembl
chr6:103440983..103520623hg19UCSC Ensembl
chr6:103547676..103627316hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3879641
hg1979641
hg1879641
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024908, nsv1032744
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)dgv6116n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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