A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651126



Internal ID21599431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104764084..104764084hg38UCSC Ensembl
chr14:105230421..105230421hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094391
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651126
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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