A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528510



Internal ID20901871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10102367..10133807hg38UCSC Ensembl
chr19:10213043..10244483hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3831441
hg1931441
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198011
Samples
Known GenesANGPTL6, DNMT1, EIF3G, P2RY11, PPAN, PPAN-P2RY11, SNORD105, SNORD105B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528510
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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