A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533932



Internal ID20907293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17862333..17966738hg38UCSC Ensembl
chr19:17973142..18077547hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38104406
hg19104406
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197711
Samples
Known GenesCCDC124, KCNN1, RPL18A, SLC5A5, SNORA68
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533932
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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