A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189321



Internal ID20756361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82042286..82048072hg38UCSC Ensembl
chr9:84657201..84662987hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg385787
hg195787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439536
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189321
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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