A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201921



Internal ID20768962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:164632909..164633280hg38UCSC Ensembl
chr1:164602146..164602517hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333775
Supporting Variants
Samples
Known GenesPBX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201921
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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