A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442003



Internal ID21099556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33670403..33860450hg38UCSC Ensembl
chr9:33670401..33860448hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38190048
hg19190048
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234522
Samples
Known GenesLOC101929688, PRSS3, PTENP1, PTENP1-AS, UBE2R2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442003
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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