A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211318



Internal ID20778358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:116119440..116558915hg38UCSC Ensembl
chr4:117040596..117480071hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38439476
hg19439476
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392443
Supporting Variants
Samples
Known GenesMIR1973
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211318
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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