A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406656



Internal ID21064209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:120463901..120466000hg38UCSC Ensembl
chr5:119799596..119801695hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212514
Samples
Known GenesPRR16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406656
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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