A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562344



Internal ID16349753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:73858185..74167309hg38UCSC Ensembl
Innerchr13:74432322..74741446hg19UCSC Ensembl
Innerchr13:73330323..73639447hg18UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38309125
hg19309125
hg18309125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv815762
Samples
Known GenesKLF12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562344
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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