A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739664



Internal ID18713910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168742962..168743142hg38UCSC Ensembl
Outerchr6:168742923..168743191hg38UCSC Ensembl
Innerchr6:169143058..169143238hg19UCSC Ensembl
Outerchr6:169143019..169143287hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540917
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739664
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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