A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552060



Internal ID16339469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103447748..103470575hg38UCSC Ensembl
Innerchr10:105207505..105230332hg19UCSC Ensembl
Innerchr10:105197495..105220322hg18UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3822828
hg1922828
hg1822828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv756078
Samples
Known GenesCALHM1, CALHM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552060
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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