A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6151n100



Internal ID22792238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137056586..137108951hg38UCSC Ensembl
chr6:137377723..137430088hg19UCSC Ensembl
chr6:137419416..137471781hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3852366
hg1952366
hg1852366
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020438, nsv1030088, nsv1022939
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)dgv6151n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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