A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499267



Internal ID20872485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103938480..103944560hg38UCSC Ensembl
chr14:104404817..104410897hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg386081
hg196081
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189961
Samples
Known GenesRD3L, TDRD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499267
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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