A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503115



Internal ID20876367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102492257..102799383hg38UCSC Ensembl
chr14:102958594..103265720hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38307127
hg19307127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181012
Samples
Known GenesANKRD9, MIR4309, RCOR1, TECPR2, TRAF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503115
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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