A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6079n100



Internal ID22792166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85764650..85856745hg38UCSC Ensembl
chr6:86474368..86566463hg19UCSC Ensembl
chr6:86531087..86623182hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3892096
hg1992096
hg1892096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031231, nsv1033419, nsv1034677, nsv1025427
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)dgv6079n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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