A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095529



Internal ID21403455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95029857..95029857hg38UCSC Ensembl
chr14:95496194..95496194hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656246
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095529
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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