A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047664



Internal ID20614704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32569220..32569465hg38UCSC Ensembl
chr19:33060126..33060371hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534489
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047664
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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