A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215900



Internal ID20782940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156658801..156665500hg38UCSC Ensembl
chr5:156085812..156092511hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411001
Supporting Variants
Samples
Known GenesSGCD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215900
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00619


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