A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762485



Internal ID18736731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39702892..39712100hg38UCSC Ensembl
Outerchr4:39701381..39713206hg38UCSC Ensembl
Innerchr4:39704512..39713720hg19UCSC Ensembl
Outerchr4:39703001..39714826hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3811826
hg1911826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563738
Supporting Variants
Samples
Known GenesUBE2K
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762485
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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