A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634928



Internal ID21826975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50083748..50083748hg38UCSC Ensembl
chr17:48161112..48161112hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg384761
hg194761
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088810
Supporting Variants
Samples
Known GenesITGA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634928
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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