A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv996874



Internal ID16290830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43378116..43683852hg38UCSC Ensembl
Innerchr4:43380133..43685869hg19UCSC Ensembl
Innerchr4:43074890..43380626hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38305737
hg19305737
hg18305737
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594095
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)nssv996874
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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