A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030544



Internal ID21939887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2834665..2940872hg38UCSC Ensembl
chr16:2884666..2990873hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38106208
hg19106208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607537
Samples
Known GenesFLYWCH1, FLYWCH2, PRSS22, PRSS30P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030544
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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