A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559955



Internal ID16000678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:99589553..99611051hg38UCSC Ensembl
Innerchr12:99983331..100004829hg19UCSC Ensembl
Innerchr12:98507462..98528960hg18UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3821499
hg1921499
hg1821499
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv801470
Samples
Known GenesANKS1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559955
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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