A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878906



Internal ID16172862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:29950742..30028891hg38UCSC Ensembl
Innerchr18:27530707..27608856hg19UCSC Ensembl
Innerchr18:25784705..25862854hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3878150
hg1978150
hg1878150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576618
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv878906
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer