A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17582440



Internal ID21774483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103816533..103816533hg38UCSC Ensembl
chr10:105576291..105576291hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6098024
Supporting Variants
Samples
Known GenesSH3PXD2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17582440
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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