A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744592



Internal ID18718838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6612800..6614033hg38UCSC Ensembl
Outerchr10:6612769..6614190hg38UCSC Ensembl
Innerchr10:6654762..6655995hg19UCSC Ensembl
Outerchr10:6654731..6656152hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381422
hg191422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545845
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744592
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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