A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929784



Internal ID22705043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36220566..36221489hg38UCSC Ensembl
chr19:36711468..36712391hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38924
hg19924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397624
Samples
Known GenesZNF146
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929784
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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