A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636029



Internal ID21584334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27698454..27698454hg38UCSC Ensembl
chr7:27738073..27738073hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158964
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636029
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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