A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903842



Internal ID22679013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:41569172..41582605hg38UCSC Ensembl
chr5:41569274..41582707hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3813434
hg1913434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416116
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903842
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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