A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17143285



Internal ID21456881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4894856..4894856hg38UCSC Ensembl
chr6:4895090..4895090hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632356
Supporting Variants
SamplesHG02587
Known GenesCDYL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17143285
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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