A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409017



Internal ID22466887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41373621..41373621hg38UCSC Ensembl
chr19:41879526..41879526hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38673
hg19673
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976846
Supporting Variants
Samples
Known GenesTMEM91
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409017
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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