A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17119237



Internal ID21499211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16149891..16150219hg38UCSC Ensembl
chr21:17522211..17522539hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593068
Supporting Variants
SamplesNA19239
Known GenesLINC00478
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17119237
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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