A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571972



Internal ID21520355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37788536..37788611hg38UCSC Ensembl
chr8:37646054..37646129hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152310
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571972
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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