A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227192



Internal ID20794232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127409601..127469900hg38UCSC Ensembl
chr9:130171880..130232179hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3860300
hg1960300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445995
Supporting Variants
Samples
Known GenesLRSAM1, RPL12, SNORA65, ZNF79
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227192
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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