A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404397



Internal ID22462267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58140733..58142529hg38UCSC Ensembl
chr20:56715789..56717585hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg381797
hg191797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963008
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404397
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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