A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606866



Internal ID21798913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30815640..30887390hg38UCSC Ensembl
chr15:31107843..31179593hg19UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3871751
hg1971751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035992
Supporting Variants
Samples
Known GenesHERC2P10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606866
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