A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236699



Internal ID20803739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76454961..76464418hg38UCSC Ensembl
chr9:79069877..79079334hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg389458
hg199458
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448854
Supporting Variants
Samples
Known GenesGCNT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236699
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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