A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6086n100



Internal ID20157702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88129212..88159329hg38UCSC Ensembl
chr6:88838931..88869048hg19UCSC Ensembl
chr6:88895650..88925767hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3830118
hg1930118
hg1830118
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1023549, nsv1020107
Samples
Known GenesCNR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6086n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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