A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931635



Internal ID22706922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:53399607..53399929hg38UCSC Ensembl
chr18:50925977..50926299hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385929
Samples
Known GenesDCC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931635
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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