A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646032



Internal ID21594337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30646401..30646401hg38UCSC Ensembl
chr14:31115607..31115607hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091720
SamplesHG03125
Known GenesSCFD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646032
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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