A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744673



Internal ID18718919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13217452..13218715hg38UCSC Ensembl
Outerchr10:13217181..13218853hg38UCSC Ensembl
Innerchr10:13259452..13260715hg19UCSC Ensembl
Outerchr10:13259181..13260853hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381673
hg191673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545926
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744673
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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