A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2721001



Internal ID10304637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:155799903..155800603hg38UCSC Ensembl
Outerchr2:156656415..156657115hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6756826, essv6817058, essv6962204, essv6933747, essv6853851, essv6906524
SamplesSSM059, SSM027, SSM087, SSM021, SSM014, SSM078
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)esv2721001
Frequency
Sample Size96
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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