A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6152n100



Internal ID22792239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137577090..137644463hg38UCSC Ensembl
chr6:137898227..137965600hg19UCSC Ensembl
chr6:137939920..138007293hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3867374
hg1967374
hg1867374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022180, nsv1034012
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)dgv6152n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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