A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573221



Internal ID21521622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167940651..167941454hg38UCSC Ensembl
chr6:168341331..168342134hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145489
SamplesHG02818
Known GenesMLLT4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573221
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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