A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409698



Internal ID21067251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:120679794..120800792hg38UCSC Ensembl
chr5:120015489..120136487hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38120999
hg19120999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212515
Samples
Known GenesPRR16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409698
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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