A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382792



Internal ID22440662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73817740..73817740hg38UCSC Ensembl
chr14:74284443..74284443hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972073
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382792
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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