A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486728



Internal ID21144281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77389750..77395357hg38UCSC Ensembl
chr14:77856093..77861700hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg385608
hg195608
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196054
Samples
Known GenesNOXRED1, SAMD15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486728
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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