A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662006



Internal ID21610311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24696967..24696967hg38UCSC Ensembl
chr14:25166173..25166173hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080637, nssv17082151
SamplesHG00731, HG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662006
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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