A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611756



Internal ID21560061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143126042..143126042hg38UCSC Ensembl
chr3:142844884..142844884hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120817
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611756
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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