A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683837



Internal ID15420489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:30223255..30282580hg38UCSC Ensembl
Innerchr18:27803220..27862545hg19UCSC Ensembl
Innerchr18:26057218..26116543hg18UCSC Ensembl
Innerchr18:26057218..26116543hg17UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3859326
hg1959326
hg1859326
hg1759326
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516109
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683837
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