A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6705928



Internal ID9772131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46271457..46271861hg38UCSC Ensembl
Outerchr10:47642693..47643097hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2736307, esv2736163, esv2736285
Supporting Variants
SamplesSSM040
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)essv6705928
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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