A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218494



Internal ID20785534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36395001..36400600hg38UCSC Ensembl
chr9:36394998..36400597hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442338
Supporting Variants
Samples
Known GenesRNF38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218494
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00064


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