A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6976563



Internal ID10081563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:44179562..44181089hg38UCSC Ensembl
Outerchr10:44675010..44676537hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg381528
hg191528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2735872
Supporting Variants
SamplesSSM029
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)essv6976563
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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