A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660263



Internal ID21608568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51178098..51178098hg38UCSC Ensembl
chr14:51644816..51644816hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094729, nssv17091678
SamplesNA19239, HG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660263
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer