A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566181



Internal ID21514503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178526150..178526502hg38UCSC Ensembl
chr1:178495285..178495637hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061389
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566181
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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