A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885238



Internal ID22660222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5112393..5113466hg38UCSC Ensembl
chr1:5172453..5173526hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg381074
hg191074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384164
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885238
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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