A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120563



Internal ID21414209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:13427568..13427568hg38UCSC Ensembl
chr5:13427680..13427680hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632597
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120563
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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