A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097141



Internal ID20664181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169955035..169956674hg38UCSC Ensembl
chr3:169672823..169674462hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg381640
hg191640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367543
Supporting Variants
Samples
Known GenesLOC100128164
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097141
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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