A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940267



Internal ID22715673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59527257..59550463hg38UCSC Ensembl
chr15:59819456..59842662hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3823207
hg1923207
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv753n209
Supporting Variantsnssv17371211
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940267
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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