A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659212



Internal ID21607517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49846029..49846029hg38UCSC Ensembl
chr17:47923391..47923391hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg381787
hg191787
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17079856
SamplesHG01596
Known GenesFLJ45513, TAC4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659212
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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