A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17119255



Internal ID21506702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16577417..16577417hg38UCSC Ensembl
chr21:17949737..17949737hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671022
Supporting Variants
SamplesNA19983
Known GenesLINC00478
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17119255
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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