A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529780



Internal ID20903141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46822962..46833957hg38UCSC Ensembl
chr19:47326219..47337214hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3810996
hg1910996
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198928
Samples
Known GenesSNAR-E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529780
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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