A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137819



Internal ID21401896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133625396..133625396hg38UCSC Ensembl
chr5:132961087..132961087hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg381215
hg191215
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634419
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137819
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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