A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416716



Internal ID21074269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19312502..19583892hg38UCSC Ensembl
chr9:19312500..19583890hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38271391
hg19271391
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236071
Samples
Known GenesACER2, DENND4C, RPS6, SLC24A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416716
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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