A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557861



Internal ID16345270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:27780309..27780963hg38UCSC Ensembl
Innerchr12:27933242..27933896hg19UCSC Ensembl
Innerchr12:27824509..27825163hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38655
hg19655
hg18655
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv790086
Samples
Known GenesKLHL42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557861
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer