A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452629



Internal ID21110182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:84170004..84196180hg38UCSC Ensembl
chr9:86784919..86811095hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3826177
hg1926177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183897
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452629
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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