A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155508



Internal ID22086013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:39380799..39431244hg38UCSC Ensembl
Outerchr18:39377776..39431781hg38UCSC Ensembl
Innerchr18:36960763..37011208hg19UCSC Ensembl
Outerchr18:36957740..37011745hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3854006
hg1954006
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011890
Samples
Known GenesLINC00669
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155508
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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