A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616836



Internal ID21565141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46329126..46329126hg38UCSC Ensembl
chr1:46794798..46794798hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065524
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616836
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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