A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661056



Internal ID21609361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56953157..56953157hg38UCSC Ensembl
chr17:55030518..55030518hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090856
SamplesHG02011
Known GenesCOIL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661056
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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