A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580150



Internal ID21772193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:106602875..106602875hg38UCSC Ensembl
chr10:108362633..108362633hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092751
Supporting Variants
Samples
Known GenesSORCS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580150
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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