A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv995847



Internal ID16289803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35274996..35354707hg38UCSC Ensembl
Innerchr4:35276618..35356329hg19UCSC Ensembl
Innerchr4:34953013..35032724hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3879712
hg1979712
hg1879712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593973
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv995847
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