A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6000n100



Internal ID22792087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:65106986..65210761hg38UCSC Ensembl
chr6:65816879..65920654hg19UCSC Ensembl
chr6:65873600..65977375hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38103776
hg19103776
hg18103776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030636, nsv1033137, nsv1017889, nsv1024620, nsv1026001
Samples
Known GenesEYS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6000n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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