A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906958



Internal ID22682162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:193255529..193255584hg38UCSC Ensembl
chr3:192973318..192973373hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429602
Samples
Known GenesHRASLS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906958
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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