A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081643



Internal ID21485894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58753666..58753666hg38UCSC Ensembl
chr14:59220384..59220384hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg386071
hg196071
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652811
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081643
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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