A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074718



Internal ID21484744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45874484..45874549hg38UCSC Ensembl
chr11:45896035..45896100hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600491
Supporting Variants
SamplesNA12329
Known GenesCRY2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074718
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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