A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3540691



Internal ID18741767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:154496317..154496508hg38UCSC Ensembl
Outerchr6:154496279..154496544hg38UCSC Ensembl
Innerchr6:154817451..154817642hg19UCSC Ensembl
Outerchr6:154817413..154817678hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9739438
Samples
Known GenesCNKSR3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3540691
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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