A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633960



Internal ID21582265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15704080..15704080hg38UCSC Ensembl
chr7:15743705..15743705hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg382177
hg192177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141154
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633960
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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