A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569734



Internal ID21518095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52301388..52306660hg38UCSC Ensembl
chr6:52166186..52171458hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg385273
hg195273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159376
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569734
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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