A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467026



Internal ID22524918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:114333611..114338519hg38UCSC Ensembl
chr13:115099086..115103994hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg384909
hg194909
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860548
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467026
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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