A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567553



Internal ID21515891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141155967..141156017hg38UCSC Ensembl
chr4:142077121..142077171hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130336
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567553
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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