A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662771



Internal ID15399423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:191950256..191957971hg38UCSC Ensembl
Innerchr3:191668045..191675760hg19UCSC Ensembl
Innerchr3:193150739..193158454hg18UCSC Ensembl
Innerchr3:193150747..193158462hg17UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg387716
hg197716
hg187716
hg177716
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517535
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662771
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