A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090949



Internal ID21473754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99347932..99347932hg38UCSC Ensembl
chr14:99814269..99814269hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644948
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090949
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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