A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082973



Internal ID21454305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27857551..27857551hg38UCSC Ensembl
chr14:28326757..28326757hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656855
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082973
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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