A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17391999



Internal ID22449869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122102869..122102932hg38UCSC Ensembl
chr3:121821716..121821779hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5899465
Supporting Variants
Samples
Known GenesCD86
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17391999
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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