A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032988



Internal ID89695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33098162..33098235hg38UCSC Ensembl
chr10:33387090..33387163hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492269
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032988
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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