A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519823



Internal ID20893184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51745501..51747200hg38UCSC Ensembl
chr19:52248754..52250453hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048746
Samples
Known GenesFPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519823
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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