A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150219



Internal ID21476652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32495327..32495327hg38UCSC Ensembl
chr7:32534939..32534939hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635803
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150219
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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