A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519122



Internal ID20892483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20247301..20618400hg38UCSC Ensembl
chr19:20358110..20801206hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38371100
hg19443097
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3461n223
Supporting Variantsnssv18198412
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF737, ZNF826P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519122
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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