A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040229



Internal ID94528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130938933..130954202hg38UCSC Ensembl
chr10:132737196..132752465hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3815270
hg1915270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501599
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040229
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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