A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10912n54



Internal ID22778807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113380637..113381508hg38UCSC Ensembl
chr6:113701839..113702710hg19UCSC Ensembl
chr6:113808532..113809403hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38872
hg19872
hg18872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604520, nsv604525, nsv604522, nsv604519, nsv604523
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10912n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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