A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17118892



Internal ID21421121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:34011407..34011407hg38UCSC Ensembl
chr21:35383708..35383708hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672089
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17118892
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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