A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932762



Internal ID22708065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29440170..29441904hg38UCSC Ensembl
chr19:29931077..29932811hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381735
hg191735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395178
Samples
Known GenesLOC284395
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932762
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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