A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275251



Internal ID348157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:139100588..139101546hg38UCSC Ensembl
Outerchr6:139099858..139103974hg38UCSC Ensembl
Innerchr6:139421725..139422683hg19UCSC Ensembl
Outerchr6:139420995..139425111hg19UCSC Ensembl
Innerchr6:139463418..139464376hg18UCSC Ensembl
Outerchr6:139462688..139466804hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg384117
hg194117
hg184117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585796
Samples
Known Genes
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv275251
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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