A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698086



Internal ID15088052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:966370..968728hg38UCSC Ensembl
Innerchr12:1075536..1077894hg19UCSC Ensembl
Innerchr12:945797..948155hg18UCSC Ensembl
Innerchr12:945797..948155hg17UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg382359
hg192359
hg182359
hg172359
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516003
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698086
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