A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532374



Internal ID20905735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11475072..11499015hg38UCSC Ensembl
chr19:11585887..11609830hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3823944
hg1923944
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198067
Samples
Known GenesELAVL3, MIR7974, ZNF653
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532374
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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