A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091488



Internal ID21478873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101658840..101658840hg38UCSC Ensembl
chr14:102125177..102125177hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660594
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091488
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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