A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629873



Internal ID21578178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5555054..5555054hg38UCSC Ensembl
chr7:5594685..5594685hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38942
hg19942
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144110
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629873
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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