A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843578



Internal ID15790848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58439368..58486840hg38UCSC Ensembl
Innerchr15:58731567..58779039hg19UCSC Ensembl
Innerchr15:56518859..56566331hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3847473
hg1947473
hg1847473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569600
Supporting Variants
Samples
Known GenesLIPC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv843578
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