A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871482



Internal ID22646420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48641210..48643647hg38UCSC Ensembl
chr19:49144467..49146904hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg382438
hg192438
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477312
Samples
Known GenesCA11, SEC1P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871482
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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