A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573227



Internal ID21521628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69324640..69324736hg38UCSC Ensembl
chr8:70236875..70236971hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147206
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573227
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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