A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097048



Internal ID21505410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96989175..96989175hg38UCSC Ensembl
chr13:97641429..97641429hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663015
Supporting Variants
SamplesNA19650
Known GenesOXGR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097048
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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