A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029941



Internal ID20596981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48878602..48880409hg38UCSC Ensembl
chr16:48912513..48914320hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg381808
hg191808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510850
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029941
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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