A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744871



Internal ID18719117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:32416813..32417128hg38UCSC Ensembl
Outerchr10:32416748..32417174hg38UCSC Ensembl
Innerchr10:32705741..32706056hg19UCSC Ensembl
Outerchr10:32705676..32706102hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546124
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744871
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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