A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572177



Internal ID21520562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15503669..15503978hg38UCSC Ensembl
chr8:15361178..15361487hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149584
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572177
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