A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706557



Internal ID21378833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52167426..52167493hg38UCSC Ensembl
chr20:50783965..50784032hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392579
Supporting Variants
Samples
Known GenesZFP64
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706557
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.117816


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