A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369799



Internal ID22595468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57966246..57966246hg38UCSC Ensembl
chr14:58432964..58432964hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970446
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369799
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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