A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9763500



Internal ID18737746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:145834166..145834796hg38UCSC Ensembl
Outerchr4:145834123..145834842hg38UCSC Ensembl
Innerchr4:146755318..146755948hg19UCSC Ensembl
Outerchr4:146755275..146755994hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564753
Supporting Variants
Samples
Known GenesZNF827
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9763500
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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