A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033679



Internal ID90143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21685615..21685615hg38UCSC Ensembl
chr10:21974544..21974544hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552334
Supporting Variants
Samples
Known GenesMLLT10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033679
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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