A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621629



Internal ID21813676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50085672..50086196hg38UCSC Ensembl
chr17:48163036..48163560hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035794
Supporting Variants
Samples
Known GenesITGA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621629
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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