A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624232



Internal ID21572537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152306380..152306380hg38UCSC Ensembl
chr1:152278856..152278856hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38972
hg19972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17060644
SamplesHG00731
Known GenesFLG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624232
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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