A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033150



Internal ID89793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36360087..36361731hg38UCSC Ensembl
chr10:36649015..36650659hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381645
hg191645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483956
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033150
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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