A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532871



Internal ID20906232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46119501..46123600hg38UCSC Ensembl
chr19:46622758..46626857hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3669n223
Supporting Variantsnssv18046564
Samples
Known GenesIGFL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532871
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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