A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518554



Internal ID20891915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51721256..51857352hg38UCSC Ensembl
chr19:52224509..52360605hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38136097
hg19136097
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198316
Samples
Known GenesFPR1, FPR2, FPR3, HAS1, ZNF577
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518554
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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