A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622558



Internal ID21570863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96570303..96570303hg38UCSC Ensembl
chr1:97035859..97035859hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067368
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622558
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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