A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095733



Internal ID21446858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101009896..101009896hg38UCSC Ensembl
chr14:101476233..101476233hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5647526
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095733
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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