A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031300



Internal ID20598340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66645427..66655151hg38UCSC Ensembl
chr16:66679330..66689054hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg389725
hg199725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515397
Supporting Variants
Samples
Known GenesCMTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031300
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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