A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932198



Internal ID22707492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61639003..61644335hg38UCSC Ensembl
chr16:61672907..61678239hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg385333
hg195333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385510
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932198
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