A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392349



Internal ID21049902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:160613463..160875061hg38UCSC Ensembl
chr4:161534615..161796213hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38261599
hg19261599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211095
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392349
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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