A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077096



Internal ID21504962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:107069559..107069612hg38UCSC Ensembl
chr12:107463337..107463390hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597598
Supporting Variants
SamplesNA19650
Known GenesCRY1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077096
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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