A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520630



Internal ID20893991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3121001..3122100hg38UCSC Ensembl
chr19:3120999..3122098hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197294
Samples
Known GenesGNA11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520630
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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