A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088288



Internal ID21455937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19517657..19517657hg38UCSC Ensembl
chr16:19528979..19528979hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645829
Supporting Variants
SamplesHG02492
Known GenesGDE1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088288
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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