A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032811



Internal ID20599851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8110901..8263277hg38UCSC Ensembl
chr16:8160903..8313279hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38152377
hg19152377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504093
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032811
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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