A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534676



Internal ID20908037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46119101..46123700hg38UCSC Ensembl
chr19:46622358..46626957hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3669n223
Supporting Variantsnssv18046562
Samples
Known GenesIGFL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534676
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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