A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144110



Internal ID21482769
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 StatusS
Merged Variantsnsv5629873
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144110
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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