A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227357



Internal ID20794397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76563392..76570288hg38UCSC Ensembl
chr9:79178308..79185204hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg386897
hg196897
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438019
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227357
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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