A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903852



Internal ID22679024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:45041330..45047639hg38UCSC Ensembl
chr5:45041432..45047741hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg386310
hg196310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428923
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903852
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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