A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762856



Internal ID18737102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:77183915..77184065hg38UCSC Ensembl
Outerchr4:77183913..77184073hg38UCSC Ensembl
Innerchr4:78105068..78105218hg19UCSC Ensembl
Outerchr4:78105066..78105226hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564109
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762856
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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