A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033677



Internal ID90141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21652069..21652124hg38UCSC Ensembl
chr10:21940998..21941053hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486435
Supporting Variants
Samples
Known GenesMLLT10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033677
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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