A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877908



Internal ID22652874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42551518..42571021hg38UCSC Ensembl
chr19:43055670..43075173hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3819504
hg1919504
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475977
Samples
Known GenesLIPE-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877908
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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