A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9766060



Internal ID18740306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:15666578..15667436hg38UCSC Ensembl
Outerchr6:15666450..15667616hg38UCSC Ensembl
Innerchr6:15666809..15667667hg19UCSC Ensembl
Outerchr6:15666681..15667847hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381167
hg191167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567313
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9766060
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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