A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503761



Internal ID20877017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58288650..58289544hg38UCSC Ensembl
chr16:58322554..58323448hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38895
hg19895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029824
Samples
Known GenesPRSS54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503761
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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