A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033436



Internal ID89980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28728918..28728957hg38UCSC Ensembl
chr10:29017847..29017886hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535346
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033436
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003903


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