A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224932



Internal ID20791972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85528187..85544583hg38UCSC Ensembl
chr9:88143102..88159498hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3816397
hg1916397
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438031
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224932
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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