A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664134



Internal ID21612439
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 StatusM
Merged Variants
Supporting Variantsnssv17089957
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664134
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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