A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028955



Internal ID20595995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31540043..31543216hg38UCSC Ensembl
chr16:31551364..31554537hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg383174
hg193174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506055
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028955
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00054


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