A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408684



Internal ID22466554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6537876..6545397hg38UCSC Ensembl
chr19:6537887..6545408hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg387522
hg197522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934190
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408684
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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