A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663598



Internal ID21611903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21260117..21260117hg38UCSC Ensembl
chr14:21728276..21728276hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38766
hg19766
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086563
SamplesHG00732
Known GenesHNRNPC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663598
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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