A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939567



Internal ID22714962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58240389..58244043hg38UCSC Ensembl
chr19:58751755..58755409hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg383655
hg193655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391028
Samples
Known GenesZNF544
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939567
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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