A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762796



Internal ID18390356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:70242283..70242469hg38UCSC Ensembl
Outerchr4:70242241..70242510hg38UCSC Ensembl
Innerchr4:71108000..71108186hg19UCSC Ensembl
Outerchr4:71107958..71108227hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564049
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762796
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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