A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6795696



Internal ID9852833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:28901684..28901843hg38UCSC Ensembl
Outerchr10:29190613..29190772hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734606, esv2734872
Supporting Variants
SamplesSSM071
Known Genes
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6795696
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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