A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966268



Internal ID22741203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44660275..44695178hg38UCSC Ensembl
chr20:43288916..43323819hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3834904
hg1934904
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395983
Samples
Known GenesLOC79015
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966268
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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