A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409795



Internal ID21067348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180941901..181088900hg38UCSC Ensembl
chr5:180368901..180515900hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38147000
hg19147000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6029n223
Supporting Variantsnssv18215169
Samples
Known GenesBTNL3, BTNL8, BTNL9, MIR8089
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409795
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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