A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585318



Internal ID211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110251072..110251726hg38UCSC Ensembl
Outerchr10:110246698..110252482hg38UCSC Ensembl
Innerchr10:112010830..112011484hg19UCSC Ensembl
Outerchr10:112006456..112012240hg19UCSC Ensembl
Innerchr10:112000820..112001474hg18UCSC Ensembl
Outerchr10:111996446..112002230hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg385785
hg195785
hg185785
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275343
Supporting Variants
Samples
Known GenesMXI1
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)essv2585318
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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