A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9745218



Internal ID18719464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69238376..69238652hg38UCSC Ensembl
Outerchr10:69238323..69238740hg38UCSC Ensembl
Innerchr10:70998132..70998408hg19UCSC Ensembl
Outerchr10:70998079..70998496hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546471
Supporting Variants
Samples
Known GenesHKDC1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9745218
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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