A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873442



Internal ID22648388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3157158..3165564hg38UCSC Ensembl
chr19:3157156..3165562hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg388407
hg198407
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474680
Samples
Known GenesGNA15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873442
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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