A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090171



Internal ID21473860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34573737..34573737hg38UCSC Ensembl
chr16:46409757..46409757hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661140
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090171
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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