A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029548



Internal ID20596588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25807901..25810200hg38UCSC Ensembl
chr16:25819222..25821521hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511936
Supporting Variants
Samples
Known GenesHS3ST4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029548
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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