A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448220



Internal ID21105773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41771401..41910400hg38UCSC Ensembl
chr9:65645562..67672498hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38139000
hg192026937
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7746n223
Supporting Variantsnssv18224689
Samples
Known GenesAQP7P1, LOC286297, PTGER4P2-CDK2AP2P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448220
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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