A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977329



Internal ID22752264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60063076..60063076hg38UCSC Ensembl
chr20:58638131..58638131hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391350
Samples
Known GenesC20orf197
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977329
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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