A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077138



Internal ID21502920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110387383..110387383hg38UCSC Ensembl
chr12:110825188..110825188hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664329
Supporting Variants
SamplesNA19239
Known GenesANAPC7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077138
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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