A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610531



Internal ID21802578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71490157..71490288hg38UCSC Ensembl
chr15:71782496..71782627hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035081
Supporting Variants
Samples
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610531
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