A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642225



Internal ID21590530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173114443..173114443hg38UCSC Ensembl
chr4:174035594..174035594hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg383225
hg193225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127305
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642225
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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