A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412265



Internal ID22470135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57968350..57992098hg38UCSC Ensembl
chr3:57954077..57977825hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3823749
hg1923749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895933
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412265
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer