A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17158713



Internal ID21441780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:117326088..117326088hg38UCSC Ensembl
chr7:116966142..116966142hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624815
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17158713
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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