A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582159



Internal ID21530669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22029136..22029289hg38UCSC Ensembl
chr7:22068754..22068907hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149421
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582159
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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