A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874284



Internal ID22649235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58470444..58480455hg38UCSC Ensembl
chr19:58981811..58991822hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3810012
hg1910012
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479340
Samples
Known GenesZNF324, ZNF446
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874284
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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