A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029753



Internal ID20596793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47897101..47906200hg38UCSC Ensembl
chr16:47931012..47940111hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg389100
hg199100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498220
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029753
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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