A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029266



Internal ID20596306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27138937..27162771hg38UCSC Ensembl
chr16:27150258..27174092hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3823835
hg1923835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508465
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029266
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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