A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089318



Internal ID21486659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7083650..7084082hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595900
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089318
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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