A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035794



Internal ID21945137
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 StatusM
Merged Variants
Supporting Variantsnssv17621629
Samples
Known GenesITGA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035794
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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