A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6695197



Internal ID9761884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:29423221..29423789hg38UCSC Ensembl
Outerchr10:29712150..29712718hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2734928, esv2734606
Supporting Variants
SamplesSSM037
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)essv6695197
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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