A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645658



Internal ID21593963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27832879..27832879hg38UCSC Ensembl
chr16:27844200..27844200hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090062
SamplesHG01114
Known GenesGSG1L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645658
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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