A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161753



Internal ID21499358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36670763..36670763hg38UCSC Ensembl
chr9:36670760..36670760hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5631750
Supporting Variants
SamplesNA19239
Known GenesMELK
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161753
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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