A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454291



Internal ID21111844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83639002..83640913hg38UCSC Ensembl
chr9:86253917..86255828hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381912
hg191912
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226946
Samples
Known GenesIDNK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454291
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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