A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698644



Internal ID15435296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113113216..113117542hg38UCSC Ensembl
Innerchr3:112832063..112836389hg19UCSC Ensembl
Innerchr3:114314753..114319079hg18UCSC Ensembl
Innerchr3:114314753..114319079hg17UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg384327
hg194327
hg184327
hg174327
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522974
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698644
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