A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025049



Internal ID21934392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:22913821..24328084hg38UCSC Ensembl
chr13:23487960..24902222hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg381414264
hg191414263
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616753
Samples
Known GenesANKRD20A19P, C1QTNF9, C1QTNF9B, C1QTNF9B-AS1, LINC00327, MIPEP, MIR2276, SACS, SACS-AS1, SGCG, SPATA13, SPATA13-AS1, TNFRSF19
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025049
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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