A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959646



Internal ID22734669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34817117..34817184hg38UCSC Ensembl
chr20:33404920..33404987hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404027
Samples
Known GenesNCOA6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959646
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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