A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033175



Internal ID89807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36603643..36609094hg38UCSC Ensembl
chr10:36892571..36898022hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg385452
hg195452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492399
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033175
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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