A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063443



Internal ID21491512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223888542..223888833hg38UCSC Ensembl
chr1:224076244..224076535hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572156
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063443
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