A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395276



Internal ID22453146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11107762..11122225hg38UCSC Ensembl
chr19:11218438..11232901hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3814464
hg1914464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935891
Supporting Variants
Samples
Known GenesLDLR, MIR6886
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395276
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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