A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585629



Internal ID347208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24802004..24829262hg38UCSC Ensembl
Outerchr9:24801542..24830702hg38UCSC Ensembl
Innerchr9:24802002..24829260hg19UCSC Ensembl
Outerchr9:24801540..24830700hg19UCSC Ensembl
Innerchr9:24792002..24819260hg18UCSC Ensembl
Outerchr9:24791540..24820700hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3829161
hg1929161
hg1829161
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275376
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)essv2585629
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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