A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139027



Internal ID21482208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138777267..138777422hg38UCSC Ensembl
chr5:138112956..138113111hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572379
Supporting Variants
SamplesHG03732
Known GenesCTNNA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139027
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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