A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615741



Internal ID21564046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:184088660..184088660hg38UCSC Ensembl
chr1:184057794..184057794hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061987
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615741
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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