A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275548



Internal ID1768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:26672709..26688681hg38UCSC Ensembl
Outerchr1:26670575..26699298hg38UCSC Ensembl
Innerchr1:26999200..27015172hg19UCSC Ensembl
Outerchr1:26997066..27025789hg19UCSC Ensembl
Innerchr1:26871787..26887759hg18UCSC Ensembl
Outerchr1:26869653..26898376hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3828724
hg1928724
hg1828724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2586060
Samples
Known GenesARID1A
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv275548
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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