A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701727



Internal ID15438379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:10578700..10596539hg38UCSC Ensembl
Innerchr18:10578697..10596536hg19UCSC Ensembl
Innerchr18:10568697..10586536hg18UCSC Ensembl
Innerchr18:10568697..10586536hg17UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3817840
hg1917840
hg1817840
hg1717840
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525588
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701727
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