A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762927



Internal ID18390487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:85643239..85643515hg38UCSC Ensembl
Outerchr4:85643193..85643583hg38UCSC Ensembl
Innerchr4:86564392..86564668hg19UCSC Ensembl
Outerchr4:86564346..86564736hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564180
Supporting Variants
Samples
Known GenesARHGAP24
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762927
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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