A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220171



Internal ID20787211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83594348..83648913hg38UCSC Ensembl
chr9:86209263..86263828hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3854566
hg1954566
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436228
Supporting Variants
Samples
Known GenesIDNK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220171
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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