A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890945



Internal ID22665976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35037250..35037321hg38UCSC Ensembl
chr5:35037355..35037426hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418385
Samples
Known GenesAGXT2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890945
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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