A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561057



Internal ID16348466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132468328..132473949hg38UCSC Ensembl
Innerchr12:133044914..133050535hg19UCSC Ensembl
Innerchr12:131554987..131560608hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg385622
hg195622
hg185622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv805832
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561057
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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