A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212797



Internal ID20779837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:177539175..177586588hg38UCSC Ensembl
chr4:178460329..178507742hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3847414
hg1947414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6387947
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212797
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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