A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18095182



Internal ID20662222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:121898501..121899105hg38UCSC Ensembl
chr3:121617348..121617952hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361564
Supporting Variants
Samples
Known GenesSLC15A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18095182
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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