A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9738533



Internal ID18712721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:56893662..56896089hg38UCSC Ensembl
Outerchr6:56893481..56896345hg38UCSC Ensembl
Innerchr6:56758460..56760887hg19UCSC Ensembl
Outerchr6:56758279..56761143hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg382865
hg192865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3539786
Supporting Variants
Samples
Known GenesDST
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9738533
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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