A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3563370



Internal ID18417760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7968969..7973155hg38UCSC Ensembl
Outerchr4:7968772..7973372hg38UCSC Ensembl
Innerchr4:7970696..7974882hg19UCSC Ensembl
Outerchr4:7970499..7975099hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg384601
hg194601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762117
Samples
Known GenesABLIM2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3563370
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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