A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089957



Internal ID21450285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101266972..101266972hg38UCSC Ensembl
chr14:101733309..101733309hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664134
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089957
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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