A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524996



Internal ID20898357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38897789..38898814hg38UCSC Ensembl
chr19:39388429..39389454hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381026
hg191026
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198113
Samples
Known GenesSIRT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524996
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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