A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv756078



Internal ID16050034
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 StatusS
Merged Variantsnsv552060
Supporting Variants
Samples
Known GenesCALHM1, CALHM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv756078
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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