A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614271



Internal ID21562576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24972770..24972770hg38UCSC Ensembl
chr1:25299261..25299261hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17064615
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614271
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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