A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614767



Internal ID21563072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88577616..88577616hg38UCSC Ensembl
chr4:89498767..89498767hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133588
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614767
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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