A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595919



Internal ID16383328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161006375..161082472hg38UCSC Ensembl
Innerchr4:161927527..162003624hg19UCSC Ensembl
Innerchr4:162146977..162223074hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3876098
hg1976098
hg1876098
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9351n54
Supporting Variantsnssv1010242
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595919
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