A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585533



Internal ID347112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:10689685..10690149hg38UCSC Ensembl
Outerchr10:10689506..10690976hg38UCSC Ensembl
Innerchr10:10731648..10732112hg19UCSC Ensembl
Outerchr10:10731469..10732939hg19UCSC Ensembl
Innerchr10:10771654..10772118hg18UCSC Ensembl
Outerchr10:10771475..10772945hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381471
hg191471
hg181471
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275408
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)essv2585533
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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