A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616826



Internal ID21565131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201642551..201642551hg38UCSC Ensembl
chr1:201611679..201611679hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062417
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616826
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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