A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661044



Internal ID21609349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24406201..24406201hg38UCSC Ensembl
chr14:24875407..24875407hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098749, nssv17080933
SamplesNA19238, NA20847
Known GenesNYNRIN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661044
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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