A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6976677



Internal ID10081460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:113678201..113679415hg38UCSC Ensembl
Outerchr10:115437960..115439174hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg381215
hg191215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2741073
Supporting Variants
SamplesSSM029
Known GenesCASP7
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)essv6976677
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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