A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881728



Internal ID22656704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105518542..105518854hg38UCSC Ensembl
chr2:106134999..106135311hg19UCSC Ensembl
Cytoband2q12.2
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401757
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881728
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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