A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084741



Internal ID21502997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27979661..27979661hg38UCSC Ensembl
chr16:27990982..27990982hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649005
Supporting Variants
SamplesNA19239
Known GenesGSG1L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084741
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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