A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17118254



Internal ID21486727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15556507..15556507hg38UCSC Ensembl
chr21:16928826..16928826hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667910
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17118254
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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