A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546676



Internal ID18747752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91439806..91455743hg38UCSC Ensembl
Outerchr10:91439244..91457676hg38UCSC Ensembl
Innerchr10:93199563..93215500hg19UCSC Ensembl
Outerchr10:93199001..93217433hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3818433
hg1918433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745423
Samples
Known GenesHECTD2, LOC100188947
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546676
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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