A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17384528



Internal ID22442398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25356582..25356582hg38UCSC Ensembl
chr14:25825788..25825788hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978471
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17384528
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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