A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6912258



Internal ID10022116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:8562643..8562878hg38UCSC Ensembl
Outerchr10:8604606..8604841hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2732506, esv2732517
Supporting Variants
SamplesSSM015
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)essv6912258
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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