A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17535454



Internal ID21859809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15611594..15611898hg38UCSC Ensembl
chr2:15751718..15752022hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5986530
Supporting Variants
Samples
Known GenesDDX1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17535454
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