A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954234



Internal ID22729487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23776407..23858056hg38UCSC Ensembl
chr20:23757044..23838693hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3881650
hg1981650
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405703
Samples
Known GenesCST2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954234
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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