A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv801559



Internal ID15748829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:99895704..99897919hg38UCSC Ensembl
Innerchr12:100289482..100291697hg19UCSC Ensembl
Innerchr12:98813613..98815828hg18UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg382216
hg192216
hg182216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559979
Supporting Variants
Samples
Known GenesANKS1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv801559
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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