A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140072



Internal ID21509586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90001606..90001666hg38UCSC Ensembl
chr8:91013834..91013894hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580935
Supporting Variants
SamplesNA20847
Known GenesDECR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140072
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