A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869431



Internal ID22644366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58188583..58190203hg38UCSC Ensembl
chr19:58699950..58701570hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg381621
hg191621
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479331
Samples
Known GenesZNF274
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869431
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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