A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576435



Internal ID16363844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:8705082..8706759hg38UCSC Ensembl
Innerchr18:8705080..8706757hg19UCSC Ensembl
Innerchr18:8695080..8696757hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381678
hg191678
hg181678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5845n54
Supporting Variantsnssv878040, nssv878039, nssv878038, nssv878037
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576435
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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