A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614479



Internal ID21562784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113372160..113372160hg38UCSC Ensembl
chr2:114129737..114129737hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg381364
hg191364
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17107569
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614479
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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