A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213569



Internal ID20780609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38958076..38960376hg38UCSC Ensembl
chr4:38959697..38961997hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382301
hg192301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392322
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213569
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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