A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140419



Internal ID21487759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:78832409..78832409hg38UCSC Ensembl
chr6:79542126..79542126hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628527
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140419
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