A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569235



Internal ID21517591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121642445..121642869hg38UCSC Ensembl
chr7:121282499..121282923hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157587
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569235
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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