A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624159



Internal ID21572464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:118263060..118263060hg38UCSC Ensembl
chr1:118805683..118805683hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17059821
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624159
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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