A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038905



Internal ID93688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125162397..125162397hg38UCSC Ensembl
chr10:126850966..126850966hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5537716
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038905
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000314


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