A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071408



Internal ID21507200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76619070..76621105hg38UCSC Ensembl
chr10:78378828..78380863hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382036
hg192036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585575
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071408
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