A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611521



Internal ID21803568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20038060..20038133hg38UCSC Ensembl
chr16:20049382..20049455hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025572
Supporting Variants
Samples
Known GenesGPR139
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611521
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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