A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606038



Internal ID21798085
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 StatusS
Merged Variantsnsv6029117
Supporting Variants
Samples
Known GenesSLCO1C1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606038
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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