A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593436



Internal ID21785479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5369831..5369831hg38UCSC Ensembl
chr10:5411794..5411794hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381086
hg191086
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085582
Supporting Variants
Samples
Known GenesUCN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593436
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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