A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141216



Internal ID21505217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:91443651..91443651hg38UCSC Ensembl
chr5:90739468..90739468hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg383821
hg193821
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630614
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141216
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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