A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488564



Internal ID21146117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61279901..61281900hg38UCSC Ensembl
chr14:61746619..61748618hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183702
Samples
Known GenesTMEM30B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488564
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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