A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275527



Internal ID348433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35623424..35623463hg38UCSC Ensembl
Outerchr10:35621058..35625108hg38UCSC Ensembl
Innerchr10:35912352..35912391hg19UCSC Ensembl
Outerchr10:35909986..35914036hg19UCSC Ensembl
Innerchr10:35952358..35952397hg18UCSC Ensembl
Outerchr10:35949992..35954042hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg384051
hg194051
hg184051
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2586104, essv2585384
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)esv275527
Frequency
Sample Size1250
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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