A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101285



Internal ID21493289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:5352036..5352095hg38UCSC Ensembl
chr18:5352035..5352094hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594877
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101285
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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