A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093487



Internal ID21478248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31712955..31712955hg38UCSC Ensembl
chr16:31724276..31724276hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650275
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093487
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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