A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211581



Internal ID20778621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:65241201..65242800hg38UCSC Ensembl
chr4:66106919..66108518hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392825
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211581
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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