A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568964



Internal ID21517317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141501047..141501421hg38UCSC Ensembl
chr4:142422200..142422574hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122184
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568964
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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