A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18095216



Internal ID20662256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122867527..122867936hg38UCSC Ensembl
chr3:122586374..122586783hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356660
Supporting Variants
Samples
Known GenesDIRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18095216
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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