A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387919



Internal ID21045472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169852173..169861134hg38UCSC Ensembl
chr4:170773324..170782285hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg388962
hg198962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213870
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387919
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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