A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275186



Internal ID348092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:29450995..29451063hg38UCSC Ensembl
Outerchr4:29449778..29453324hg38UCSC Ensembl
Innerchr4:29452617..29452685hg19UCSC Ensembl
Outerchr4:29451400..29454946hg19UCSC Ensembl
Innerchr4:29061715..29061783hg18UCSC Ensembl
Outerchr4:29060498..29064044hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg383547
hg193547
hg183547
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585915
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)esv275186
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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