A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215575



Internal ID20782615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132102422..132125809hg38UCSC Ensembl
chr6:132423562..132446949hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3823388
hg1923388
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604336
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215575
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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