A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941794



Internal ID22717224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38297032..38297645hg38UCSC Ensembl
chr19:38787672..38788285hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38614
hg19614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392539
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941794
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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