A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6833662



Internal ID9886905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:179217672..179217836hg38UCSC Ensembl
Outerchr5:178644673..178644837hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731276, esv2731275
Supporting Variants
SamplesSSM082
Known GenesADAMTS2
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)essv6833662
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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