A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402546



Internal ID22460416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46787645..46788632hg38UCSC Ensembl
chr20:45416284..45417271hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38988
hg19988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5952923
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402546
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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