A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507511



Internal ID20880803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2780325..2806304hg38UCSC Ensembl
chr16:2830326..2856305hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3825980
hg1925980
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180451
Samples
Known GenesPRSS33, PRSS41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507511
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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