A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631571



Internal ID21579876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2386586..2386586hg38UCSC Ensembl
chr7:2426221..2426221hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149105
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631571
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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