A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576789



Internal ID16364198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:44396921..44405546hg38UCSC Ensembl
Innerchr18:41976886..41985511hg19UCSC Ensembl
Innerchr18:40230884..40239509hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg388626
hg198626
hg188626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5912n54
Supporting Variantsnssv882583
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576789
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