A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744562



Internal ID18718808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5206692..5206793hg38UCSC Ensembl
Outerchr10:5206690..5206810hg38UCSC Ensembl
Innerchr10:5248655..5248756hg19UCSC Ensembl
Outerchr10:5248653..5248773hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545815
Supporting Variants
Samples
Known GenesAKR1C4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744562
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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