A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704213



Internal ID15094179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12003336..12040700hg38UCSC Ensembl
Innerchr8:11860845..11898209hg19UCSC Ensembl
Innerchr8:11898254..11935618hg18UCSC Ensembl
Innerchr8:11898254..11935618hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3837365
hg1937365
hg1837365
hg1737365
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516685
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704213
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