A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944323



Internal ID22719786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33872112..33872227hg38UCSC Ensembl
chr19:34363017..34363132hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396740
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944323
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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