A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744816



Internal ID18372376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:27823862..27824159hg38UCSC Ensembl
Outerchr10:27823808..27824211hg38UCSC Ensembl
Innerchr10:28112791..28113088hg19UCSC Ensembl
Outerchr10:28112737..28113140hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546069
Supporting Variants
Samples
Known GenesARMC4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744816
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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