A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956119



Internal ID22731311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34266071..34266389hg38UCSC Ensembl
chr20:32853877..32854195hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397617
Samples
Known GenesASIP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956119
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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