A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871368



Internal ID22646306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65177220..65184859hg38UCSC Ensembl
chr2:65404354..65411993hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg387640
hg197640
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398251
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871368
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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