A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389722



Internal ID21047275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69999512..70007045hg38UCSC Ensembl
chr4:70865229..70872762hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg387534
hg197534
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211705
Samples
Known GenesSTATH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389722
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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