A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028951



Internal ID20595991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31423273..31425099hg38UCSC Ensembl
chr16:31434594..31436420hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381827
hg191827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514649
Supporting Variants
Samples
Known GenesITGAD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028951
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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