A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965932



Internal ID22740867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36959544..36962756hg38UCSC Ensembl
chr21:38331844..38335056hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg383213
hg193213
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401490
Samples
Known GenesHLCS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965932
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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