A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6838319



Internal ID9891472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:37505935..37506232hg38UCSC Ensembl
Outerchr10:37794863..37795160hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2735595, esv2735517
Supporting Variants
SamplesSSM083
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)essv6838319
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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