A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904341



Internal ID22679518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35259411..35262075hg38UCSC Ensembl
chr5:35259513..35262177hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg382665
hg192665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904341
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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