A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401005



Internal ID22458875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:121921377..121921755hg38UCSC Ensembl
chr3:121640224..121640602hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5893604
Supporting Variants
Samples
Known GenesSLC15A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401005
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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