A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403128



Internal ID22460998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126976042..126981191hg38UCSC Ensembl
chr3:126694885..126700034hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg385150
hg195150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897282
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403128
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