A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209459



Internal ID20776499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103787385..103801732hg38UCSC Ensembl
chr4:104708542..104722889hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3814348
hg1914348
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392716
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209459
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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