A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076747



Internal ID21473427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108656229..108656315hg38UCSC Ensembl
chr12:109050005..109050091hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590324
Supporting Variants
SamplesHG03371
Known GenesCORO1C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076747
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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