A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6071n100



Internal ID22792158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80428294..80508151hg38UCSC Ensembl
chr6:81138011..81217868hg19UCSC Ensembl
chr6:81194730..81274587hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3879858
hg1979858
hg1879858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019932, nsv1018028
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)dgv6071n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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