A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333775



Internal ID20866956
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 StatusM
Merged Variants
Supporting Variantsnssv18201921
Samples
Known GenesPBX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333775
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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