A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2735528



Internal ID9969858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:36641873..36642086hg38UCSC Ensembl
Outerchr10:36930801..36931014hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6695205, essv6702107, essv6827378
SamplesSSM039, SSM080, SSM037
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)esv2735528
Frequency
Sample Size96
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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