A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275556



Internal ID348462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69213653..69213685hg38UCSC Ensembl
Outerchr10:69211705..69216160hg38UCSC Ensembl
Innerchr10:70973409..70973441hg19UCSC Ensembl
Outerchr10:70971461..70975916hg19UCSC Ensembl
Innerchr10:70643415..70643447hg18UCSC Ensembl
Outerchr10:70641467..70645922hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg384456
hg194456
hg184456
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585922
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)esv275556
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer