A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762963



Internal ID18737209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:88601810..88602069hg38UCSC Ensembl
Outerchr4:88601745..88602108hg38UCSC Ensembl
Innerchr4:89522961..89523220hg19UCSC Ensembl
Outerchr4:89522896..89523259hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564216
Supporting Variants
Samples
Known GenesHERC3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762963
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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