A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040152



Internal ID94477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130290982..130297412hg38UCSC Ensembl
chr10:132089246..132095676hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg386431
hg196431
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147025
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040152
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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