A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv802793



Internal ID16096749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:115012756..115038948hg38UCSC Ensembl
Innerchr12:115450561..115476753hg19UCSC Ensembl
Innerchr12:113934944..113961136hg18UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg3826193
hg1926193
hg1826193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560295
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv802793
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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