A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17605769



Internal ID21797816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44030899..44051252hg38UCSC Ensembl
chr15:44323097..44343450hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3820354
hg1920354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022619
Supporting Variants
Samples
Known GenesFRMD5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17605769
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