A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192948



Internal ID20759988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3055722..3075599hg38UCSC Ensembl
chr16:3105723..3125600hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3819878
hg1919878
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513244
Supporting Variants
Samples
Known GenesIL32, MMP25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192948
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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