A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5570767



Internal ID21519137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42072730..42073044hg38UCSC Ensembl
chr8:41930248..41930562hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150991
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5570767
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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