A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499290



Internal ID20872509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99480901..99486400hg38UCSC Ensembl
chr14:99947238..99952737hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193781
Samples
Known GenesCCNK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499290
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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