A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875193



Internal ID22650150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68087446..68091052hg38UCSC Ensembl
chr2:68314578..68318184hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg383607
hg193607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406106
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875193
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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