A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528784



Internal ID20902145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54217401..54275100hg38UCSC Ensembl
chr19:54721270..54778954hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3857700
hg1957685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3717n223
Supporting Variantsnssv18048869
Samples
Known GenesLILRA6, LILRB2, LILRB3, LILRB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528784
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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