A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371899



Internal ID22597568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75299938..75299938hg38UCSC Ensembl
chr14:75766641..75766641hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968238
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371899
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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