A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409834



Internal ID22467704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49837621..49837921hg38UCSC Ensembl
chr3:49875054..49875354hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5902398
Supporting Variants
Samples
Known GenesTRAIP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409834
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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