A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360281



Internal ID21017834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46800901..46840400hg38UCSC Ensembl
chr3:46842391..46881890hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3839500
hg1939500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209291
Samples
Known GenesPRSS42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360281
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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