A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535439



Internal ID20908800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20205179..20645428hg38UCSC Ensembl
chr19:20315988..20828234hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38440250
hg19512247
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3461n223
Supporting Variantsnssv18198407
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF626, ZNF737, ZNF826P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535439
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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