A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533996



Internal ID20907357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:23679796..23680111hg38UCSC Ensembl
chr19:23862598..23862913hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198536
Samples
Known GenesZNF675
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533996
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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