A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617601



Internal ID21809648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10029182..10029254hg38UCSC Ensembl
chr20:10009830..10009902hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052846
Supporting Variants
Samples
Known GenesSNAP25-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617601
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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