A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179127



Internal ID20746167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52929301..52936500hg38UCSC Ensembl
chr16:52963213..52970412hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508471
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179127
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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