A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527444



Internal ID20900805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49206517..49229305hg38UCSC Ensembl
chr19:49709774..49732562hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3822789
hg1922789
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198237
Samples
Known GenesTRPM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527444
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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