A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406952



Internal ID22464822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63617730..63618017hg38UCSC Ensembl
chr20:62249083..62249370hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5947853
Supporting Variants
Samples
Known GenesGMEB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406952
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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