A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371782



Internal ID22597451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76518519..76518519hg38UCSC Ensembl
chr14:76984862..76984862hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970543
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371782
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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