A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18030079



Internal ID20597119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4123146..4131073hg38UCSC Ensembl
chr16:4173147..4181074hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg387928
hg197928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501336
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18030079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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