A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180797



Internal ID20747837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20956977..20962937hg38UCSC Ensembl
chr16:20968299..20974259hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg385961
hg195961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500333
Supporting Variants
Samples
Known GenesDNAH3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180797
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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