A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875507



Internal ID22650464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11113123..11116944hg38UCSC Ensembl
chr19:11223799..11227620hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383822
hg193822
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472643
Samples
Known GenesLDLR, MIR6886
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875507
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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