A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17134285



Internal ID21487465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159268053..159268053hg38UCSC Ensembl
chr5:158695061..158695061hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632624
Supporting Variants
SamplesNA18534
Known GenesUBLCP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17134285
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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