A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155304



Internal ID21508087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122913500..122913500hg38UCSC Ensembl
chr7:122553554..122553554hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643223
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155304
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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