A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888385



Internal ID22663390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241687708..241689062hg38UCSC Ensembl
chr2:242627123..242628477hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381355
hg191355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393592
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888385
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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