A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568358



Internal ID21516705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44066584..44066736hg38UCSC Ensembl
chr6:44034321..44034473hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152693
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568358
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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