A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989611



Internal ID21898954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63808782..63808940hg38UCSC Ensembl
chr2:64035916..64036074hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524109
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989611
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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