A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126254



Internal ID21414650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15942538..15942888hg38UCSC Ensembl
chr5:15942647..15942997hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572473
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126254
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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