A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047542



Internal ID20614582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30526427..30526743hg38UCSC Ensembl
chr19:31017334..31017650hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519078
Supporting Variants
Samples
Known GenesZNF536
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047542
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.11063


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