A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408616



Internal ID21066169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180902501..180910000hg38UCSC Ensembl
chr5:180329501..180337000hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6027n223
Supporting Variantsnssv18215163
Samples
Known GenesBTNL8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408616
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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