A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661943



Internal ID15398595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:157808407..157809867hg38UCSC Ensembl
Innerchr4:158729559..158731019hg19UCSC Ensembl
Innerchr4:158949009..158950469hg18UCSC Ensembl
Innerchr4:159087164..159088624hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381461
hg191461
hg181461
hg171461
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517103
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661943
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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