A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935635



Internal ID22710979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7288958..7289601hg38UCSC Ensembl
chr20:7269605..7270248hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403094
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935635
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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