A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873895



Internal ID22648844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32068154..32084230hg38UCSC Ensembl
chr2:32293223..32309299hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3816077
hg1916077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404288
Samples
Known GenesSPAST
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873895
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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