A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878468



Internal ID16172424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15047754..15130159hg38UCSC Ensembl
Innerchr18:15047753..15130158hg19UCSC Ensembl
Innerchr18:15037753..15120158hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3882406
hg1982406
hg1882406
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576546
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)nssv878468
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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