A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9745253



Internal ID18719499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73417852..73418164hg38UCSC Ensembl
Outerchr10:73417807..73418195hg38UCSC Ensembl
Innerchr10:75177610..75177922hg19UCSC Ensembl
Outerchr10:75177565..75177953hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546506
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9745253
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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