A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405334



Internal ID21062887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56908242..56927639hg38UCSC Ensembl
chr5:56204069..56223466hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3819398
hg1919398
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214076
Samples
Known GenesMIER3, SETD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405334
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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