A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029191



Internal ID20596231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30836045..30849079hg38UCSC Ensembl
chr16:30847366..30860400hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3813035
hg1913035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497125
Supporting Variants
Samples
Known GenesBCL7C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029191
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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