A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084891



Internal ID21504790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43975792..43975792hg38UCSC Ensembl
chr17:42053160..42053160hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5657509
Supporting Variants
SamplesNA19650
Known GenesPYY
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084891
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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