A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6015n100



Internal ID19016383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73590773..73714632hg38UCSC Ensembl
chr6:74300496..74424355hg19UCSC Ensembl
chr6:74357217..74481076hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38123860
hg19123860
hg18123860
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029927, nsv1027691
Samples
Known GenesCD109, SLC17A5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6015n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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