A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17147656



Internal ID21482382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19687329..19687644hg38UCSC Ensembl
chr7:19726952..19727267hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566293
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17147656
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