A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152110



Internal ID21503603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90706472..90706752hg38UCSC Ensembl
chr5:90002289..90002569hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571532
Supporting Variants
SamplesNA19239
Known GenesGPR98
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152110
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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