A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744714



Internal ID18718960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17269077..17273254hg38UCSC Ensembl
Outerchr10:17268502..17274001hg38UCSC Ensembl
Innerchr10:17311076..17315253hg19UCSC Ensembl
Outerchr10:17310501..17316000hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545967
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744714
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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