A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406541



Internal ID21064094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133046242..133053383hg38UCSC Ensembl
chr5:132381934..132389075hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg387142
hg197142
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215871
Samples
Known GenesHSPA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406541
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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