A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17119096



Internal ID21403897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37122424..37122424hg38UCSC Ensembl
chr21:38494724..38494724hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670425
Supporting Variants
SamplesHG00512
Known GenesTTC3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17119096
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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