A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946635



Internal ID22722129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34354509..34358194hg38UCSC Ensembl
chr19:34845414..34849099hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg383686
hg193686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405699
Samples
Known GenesKIAA0355
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946635
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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