A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029117



Internal ID21938460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:20732135..20732832hg38UCSC Ensembl
chr12:20885069..20885766hg19UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg38698
hg19698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606038
Samples
Known GenesSLCO1C1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029117
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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