A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565319



Internal ID21513631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59729640..59773255hg38UCSC Ensembl
chr8:60642199..60685814hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3843616
hg1943616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148075
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565319
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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