A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18126675



Internal ID20693715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162171940..162185500hg38UCSC Ensembl
chr5:161598946..161612506hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3813561
hg1913561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6397112
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18126675
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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