A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv801911



Internal ID16095867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:108467757..108469062hg38UCSC Ensembl
Innerchr12:108861534..108862839hg19UCSC Ensembl
Innerchr12:107385664..107386969hg18UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381306
hg191306
hg181306
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560104
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)nssv801911
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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