A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6920929



Internal ID9987091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:236793023..236793613hg38UCSC Ensembl
Outerchr2:237701666..237702256hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2721711
Supporting Variants
SamplesSSM003
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)essv6920929
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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