A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762925



Internal ID18390485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:85541145..85541449hg38UCSC Ensembl
Outerchr4:85541112..85541502hg38UCSC Ensembl
Innerchr4:86462298..86462602hg19UCSC Ensembl
Outerchr4:86462265..86462655hg19UCSC 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 Variantsesv3564178
Supporting Variants
Samples
Known GenesARHGAP24
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762925
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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