A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033511



Internal ID90027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29992165..29992268hg38UCSC Ensembl
chr10:30281094..30281197hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492344
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033511
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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