A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589640



Internal ID21781683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104409276..104409276hg38UCSC Ensembl
chr10:106169034..106169034hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6082385
Supporting Variants
Samples
Known GenesCCDC147
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589640
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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