A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644602



Internal ID21592907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27828111..27828111hg38UCSC Ensembl
chr16:27839432..27839432hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091035
SamplesNA19239
Known GenesGSG1L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644602
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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