A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625015



Internal ID21817062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15363303..15363610hg38UCSC Ensembl
chr19:15474114..15474421hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056227
Supporting Variants
Samples
Known GenesAKAP8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625015
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