A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512720



Internal ID20886057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2778366..2792889hg38UCSC Ensembl
chr16:2828367..2842890hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3814524
hg1914524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029298
Samples
Known GenesPRSS33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512720
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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