A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053674



Internal ID21962907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62452345..62452345hg38UCSC Ensembl
chr2:62679480..62679480hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535285
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053674
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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