A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881458



Internal ID22656433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63833147..63835283hg38UCSC Ensembl
chr2:64060281..64062417hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg382137
hg192137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399324
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881458
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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