A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405351



Internal ID21062904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161240201..161248900hg38UCSC Ensembl
chr5:160667208..160675907hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215943
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405351
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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