A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213597



Internal ID20780637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39957953..40097151hg38UCSC Ensembl
chr4:39959573..40098771hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38139199
hg19139199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383770
Supporting Variants
Samples
Known GenesLOC344967, N4BP2, PDS5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213597
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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