A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497501



Internal ID20870708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103938003..103952944hg38UCSC Ensembl
chr14:104404340..104419281hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3814942
hg1914942
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192025
Samples
Known GenesRD3L, TDRD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497501
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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