A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535254



Internal ID20908615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53751627..53794880hg38UCSC Ensembl
chr19:54254881..54298134hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3843254
hg1943254
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200219
Samples
Known GenesMIR1283-2, MIR371A, MIR371B, MIR372, MIR373, MIR516A1, MIR516A2, MIR519A1, MIR519A2, MIR527, NLRP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535254
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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