A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660095



Internal ID21608400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27246963..27246963hg38UCSC Ensembl
chr16:27258284..27258284hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098854
SamplesHG03486
Known GenesNSMCE1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660095
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