A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9738728



Internal ID18712916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:73711543..73711815hg38UCSC Ensembl
Outerchr6:73711483..73711866hg38UCSC Ensembl
Innerchr6:74421266..74421538hg19UCSC Ensembl
Outerchr6:74421206..74421589hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3539981
Supporting Variants
Samples
Known GenesCD109
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9738728
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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