A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929418



Internal ID22704671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37316429..37316721hg38UCSC Ensembl
chr19:37807331..37807623hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17408306
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929418
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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