A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616116



Internal ID21564421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95005419..95005419hg38UCSC Ensembl
chr1:95470975..95470975hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067164
SamplesNA19238
Known GenesALG14
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616116
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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