A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512349



Internal ID20885682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103896401..103896949hg38UCSC Ensembl
chr14:104362738..104363286hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179397
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512349
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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