A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157991



Internal ID21498661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64407931..64407997hg38UCSC Ensembl
chr8:65320488..65320554hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570450
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157991
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