A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17109985



Internal ID21509344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206172686..206172778hg38UCSC Ensembl
chr2:207037410..207037502hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570840
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17109985
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