A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870946



Internal ID22645883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1797487..1799750hg38UCSC Ensembl
chr19:1797486..1799749hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382264
hg192264
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473327
Samples
Known GenesATP8B3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870946
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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