A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088617



Internal ID21455131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55646460..55646460hg38UCSC Ensembl
chr14:56113178..56113178hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5657333
Supporting Variants
SamplesHG02011
Known GenesKTN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088617
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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