A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5570278



Internal ID21518642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145132055..145132590hg38UCSC Ensembl
chr4:146053207..146053742hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137961
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5570278
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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