A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560404



Internal ID16001127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:119988665..119989599hg38UCSC Ensembl
Innerchr12:120426469..120427403hg19UCSC Ensembl
Innerchr12:118910852..118911786hg18UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38935
hg19935
hg18935
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv803333
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560404
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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