A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843579



Internal ID16137535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58508567..58573957hg38UCSC Ensembl
Innerchr15:58800766..58866156hg19UCSC Ensembl
Innerchr15:56588058..56653448hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3865391
hg1965391
hg1865391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569601
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)nssv843579
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