A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627020



Internal ID21575325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186299775..186299775hg38UCSC Ensembl
chr4:187220929..187220929hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133165
SamplesHG00731
Known GenesF11-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627020
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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