A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18133313



Internal ID20700353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69023001..69031500hg38UCSC Ensembl
chr5:68318828..68327327hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412611
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18133313
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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