A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495858



Internal ID20869053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102530726..102542193hg38UCSC Ensembl
chr14:102997063..103008530hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3811468
hg1911468
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186270
Samples
Known GenesMIR4309
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495858
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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