A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375914



Internal ID22601583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81252880..81252880hg38UCSC Ensembl
chr14:81719224..81719224hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968844
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375914
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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