A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569303



Internal ID21517659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88283210..88283267hg38UCSC Ensembl
chr6:88992929..88992986hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155066
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569303
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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