A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089086



Internal ID21474481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94607234..94607234hg38UCSC Ensembl
chr13:95259488..95259488hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650533
Supporting Variants
SamplesHG03371
Known GenesGPR180
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089086
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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