A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564182



Internal ID18418572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:85739620..85739920hg38UCSC Ensembl
Outerchr4:85739562..85739964hg38UCSC Ensembl
Innerchr4:86660773..86661073hg19UCSC Ensembl
Outerchr4:86660715..86661117hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762929
Samples
Known GenesARHGAP24
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564182
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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