A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565457



Internal ID21513770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48058301..48058357hg38UCSC Ensembl
chr4:48060318..48060374hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138135
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565457
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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