A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6113n100



Internal ID22792200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:100643558..100709617hg38UCSC Ensembl
chr6:101091434..101157493hg19UCSC Ensembl
chr6:101198155..101264214hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3866060
hg1966060
hg1866060
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031817, nsv1028583, nsv1015465, nsv1032826
Samples
Known GenesASCC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6113n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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