A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562820



Internal ID335761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21685585..21687043hg38UCSC Ensembl
chr10:21974514..21975972hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381459
hg191459
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033678
Samples
Known GenesMLLT10
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562820
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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