A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428633



Internal ID21086186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5306001..5338800hg38UCSC Ensembl
chr9:5306001..5338800hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3832800
hg1932800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7549n223
Supporting Variantsnssv18229025
Samples
Known GenesRLN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428633
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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