A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887102



Internal ID22662094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42529579..42532265hg38UCSC Ensembl
chr19:43033731..43036417hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382687
hg192687
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475974
Samples
Known GenesLIPE-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887102
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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