A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088381



Internal ID21509282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80021524..80021766hg38UCSC Ensembl
chr13:80595659..80595901hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585359
Supporting Variants
SamplesNA20847
Known GenesLINC01080
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088381
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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