A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451192



Internal ID21108745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82827576..82827906hg38UCSC Ensembl
chr9:85442491..85442821hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186829
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451192
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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