A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093637



Internal ID21453217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91517487..91517487hg38UCSC Ensembl
chr14:91983831..91983831hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661329
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093637
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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