A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405597



Internal ID21063150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156660101..156666900hg38UCSC Ensembl
chr5:156087112..156093911hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5999n223
Supporting Variantsnssv18215902
Samples
Known GenesSGCD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405597
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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