A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181072



Internal ID20748112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29293046..29328609hg38UCSC Ensembl
chr16:29304367..29339930hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3835564
hg1935564
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509164
Supporting Variants
Samples
Known GenesSNX29P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181072
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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