A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950405



Internal ID21370474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:53885184..53885246hg38UCSC Ensembl
chr18:51411554..51411616hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15176325
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950405
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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