A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17034332



Internal ID90582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:56567524..56724586hg38UCSC Ensembl
chr10:58327284..58484346hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38157063
hg19157063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484975
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17034332
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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