A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934521



Internal ID22709849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34818077..34818794hg38UCSC Ensembl
chr19:35308981..35309698hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401372
Samples
Known GenesLOC400685
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934521
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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