A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236065



Internal ID20803105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121681854..121686789hg38UCSC Ensembl
chr9:124444133..124449068hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg384936
hg194936
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444691
Supporting Variants
Samples
Known GenesDAB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236065
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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