A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529920



Internal ID20903281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8110180..8119945hg38UCSC Ensembl
chr19:8175064..8184829hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg389766
hg199766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049413
Samples
Known GenesFBN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529920
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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