A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568888



Internal ID21517240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114075875..114077903hg38UCSC Ensembl
chr7:113715930..113717958hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg382029
hg192029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158851
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568888
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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