A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5621877



Internal ID21570182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151031315..151031315hg38UCSC Ensembl
chr3:150749102..150749102hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126186
SamplesNA19650
Known GenesCLRN1-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5621877
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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