A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9766446



Internal ID18740692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:41897065..41897593hg38UCSC Ensembl
Outerchr6:41896909..41897727hg38UCSC Ensembl
Innerchr6:41864803..41865331hg19UCSC Ensembl
Outerchr6:41864647..41865465hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38819
hg19819
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567699
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9766446
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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