A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3540703



Internal ID18741779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:154991339..154992705hg38UCSC Ensembl
Outerchr6:154991048..154993065hg38UCSC Ensembl
Innerchr6:155312473..155313839hg19UCSC Ensembl
Outerchr6:155312182..155314199hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg382018
hg192018
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9739450
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3540703
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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