A curated catalogue of human genomic structural variation




Variant Details

Variant: esv274890



Internal ID1110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:78105504..78109463hg38UCSC Ensembl
Outerchr15:78104105..78109916hg38UCSC Ensembl
Innerchr15:78397846..78401805hg19UCSC Ensembl
Outerchr15:78396447..78402258hg19UCSC Ensembl
Innerchr15:76184901..76188860hg18UCSC Ensembl
Outerchr15:76183502..76189313hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg385812
hg195812
hg185812
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585336, essv2585767
Samples
Known GenesCIB2
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv274890
Frequency
Sample Size1250
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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