A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882267



Internal ID22657244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4620843..4624270hg38UCSC Ensembl
chr2:4668433..4671860hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg383428
hg193428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882267
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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