A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579484



Internal ID21527965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:50350466..50350625hg38UCSC Ensembl
chr8:51263026..51263185hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157179
SamplesNA19238
Known GenesSNTG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579484
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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