A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214666



Internal ID20781707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31314668..31354309hg38UCSC Ensembl
chr4:31316290..31355931hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3839642
hg1939642
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358019
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214666
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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