A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403661



Internal ID21061214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122068446..122176041hg38UCSC Ensembl
chr5:121404141..121511736hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38107596
hg19107596
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213129
Samples
Known GenesLOC100505841, LOX, ZNF474
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403661
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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