A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177612



Internal ID20744652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66695701..66699500hg38UCSC Ensembl
chr16:66729604..66733403hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505056
Supporting Variants
Samples
Known GenesCMTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177612
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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