A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17400389



Internal ID22458259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18387813..18387813hg38UCSC Ensembl
chr19:18498623..18498623hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971291
Supporting Variants
Samples
Known GenesGDF15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17400389
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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