A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041044



Internal ID95068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110144094..110146481hg38UCSC Ensembl
chr10:111903852..111906239hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg382388
hg192388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499344
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041044
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001561


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