A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559989



Internal ID16000712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:99896242..99897919hg38UCSC Ensembl
Innerchr12:100290020..100291697hg19UCSC Ensembl
Innerchr12:98814151..98815828hg18UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381678
hg191678
hg181678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2831n54
Supporting Variantsnssv801649, nssv801650, nssv801648
Samples
Known GenesANKS1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559989
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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