A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626967



Internal ID21575272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:83871369..83871369hg38UCSC Ensembl
chr7:83500685..83500685hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153268
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626967
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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