A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881537



Internal ID22656513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25122023..25125446hg38UCSC Ensembl
chr2:25344892..25348315hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg383424
hg193424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403598
Samples
Known GenesEFR3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881537
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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