A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700839



Internal ID15437491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:190185529..190192283hg38UCSC Ensembl
Innerchr3:189903318..189910072hg19UCSC Ensembl
Innerchr3:191386012..191392766hg18UCSC Ensembl
Innerchr3:191386020..191392774hg17UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg386755
hg196755
hg186755
hg176755
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524837
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700839
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