A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611279



Internal ID21803326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90077300..90077376hg38UCSC Ensembl
chr15:90620532..90620608hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020493
Supporting Variants
Samples
Known GenesZNF710
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611279
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