A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651798



Internal ID21600103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27355268..27355268hg38UCSC Ensembl
chr17:25682294..25682294hg19UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg383491
hg193491
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089541
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651798
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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