A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585516



Internal ID347095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4199201..4199380hg38UCSC Ensembl
Outerchr10:4198678..4201806hg38UCSC Ensembl
Innerchr10:4241393..4241572hg19UCSC Ensembl
Outerchr10:4240870..4243998hg19UCSC Ensembl
Innerchr10:4231393..4231572hg18UCSC Ensembl
Outerchr10:4230870..4233998hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383129
hg193129
hg183129
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275205
Supporting Variants
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)essv2585516
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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