A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634103



Internal ID21826150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82081884..82081943hg38UCSC Ensembl
chr17:80039760..80039819hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038339
Supporting Variants
Samples
Known GenesFASN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634103
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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