A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567626



Internal ID18768702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35425235..35425354hg38UCSC Ensembl
Outerchr6:35425222..35425363hg38UCSC Ensembl
Innerchr6:35393012..35393131hg19UCSC Ensembl
Outerchr6:35392999..35393140hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9766373
Samples
Known GenesPPARD
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567626
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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