A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876780



Internal ID22651741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12033837..12039638hg38UCSC Ensembl
chr19:12144652..12150453hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385802
hg195802
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473166
Samples
Known GenesZNF433
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876780
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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