A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155901



Internal ID21401776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21189322..21189322hg38UCSC Ensembl
chr7:21228941..21228941hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639402
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155901
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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