A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151407



Internal ID15533190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62315508..62378340hg38UCSC Ensembl
Innerchr20:60890564..60953396hg19UCSC Ensembl
Innerchr20:60323959..60386791hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3862833
hg1962833
hg1862833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586486
Supporting Variants
SamplesNINDS_119
Known GenesLAMA5, MIR4758
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151407
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