A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568536



Internal ID21516885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156143847..156143951hg38UCSC Ensembl
chr7:155936541..155936645hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144289
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568536
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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