A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567700



Internal ID18768776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:41897155..41897572hg38UCSC Ensembl
Outerchr6:41897048..41897627hg38UCSC Ensembl
Innerchr6:41864893..41865310hg19UCSC Ensembl
Outerchr6:41864786..41865365hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv386e215
Supporting Variantsessv9766447
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567700
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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