A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275080



Internal ID347986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12982779..12984486hg38UCSC Ensembl
Outerchr11:12981653..12985174hg38UCSC Ensembl
Innerchr11:13004326..13006033hg19UCSC Ensembl
Outerchr11:13003200..13006721hg19UCSC Ensembl
Innerchr11:12960902..12962609hg18UCSC Ensembl
Outerchr11:12959776..12963297hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg383522
hg193522
hg183522
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585236, essv2585762
Samples
Known GenesLINC00958
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv275080
Frequency
Sample Size1250
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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