A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17384972



Internal ID22442842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101100906..101100906hg38UCSC Ensembl
chr14:101567243..101567243hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977900
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17384972
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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