A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029692



Internal ID20596732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:46816557..46817354hg38UCSC Ensembl
chr16:46850469..46851266hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507720
Supporting Variants
Samples
Known GenesC16orf87
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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