A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964384



Internal ID22739319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45915383..45915558hg38UCSC Ensembl
chr20:44544022..44544197hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396088
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964384
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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