A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560396



Internal ID16001119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:119299977..119327860hg38UCSC Ensembl
Innerchr12:119737782..119765665hg19UCSC Ensembl
Innerchr12:118222165..118250048hg18UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg3827884
hg1927884
hg1827884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176332
SamplesHGDP01378
Known GenesLINC00934
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560396
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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