A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452212



Internal ID21109765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82398747..82399305hg38UCSC Ensembl
chr9:85013662..85014220hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452212
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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