A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576809



Internal ID21525252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41930970..41931021hg38UCSC Ensembl
chr6:41898708..41898759hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145420
SamplesNA18534
Known GenesBYSL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576809
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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