A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6094n100



Internal ID22792181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:94029360..94496222hg38UCSC Ensembl
chr6:94739078..95205940hg19UCSC Ensembl
chr6:94795799..95262661hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38466863
hg19466863
hg18466863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018533, nsv1022776
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)dgv6094n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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