A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9745266



Internal ID18372826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:75213186..75213305hg38UCSC Ensembl
Outerchr10:75213183..75213308hg38UCSC Ensembl
Innerchr10:76972944..76973063hg19UCSC Ensembl
Outerchr10:76972941..76973066hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546519
Supporting Variants
Samples
Known GenesVDAC2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9745266
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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