A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030428



Internal ID87995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17567673..17584284hg38UCSC Ensembl
chr10:17609672..17626283hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3816612
hg1916612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487085
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030428
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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