A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111753



Internal ID22020986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20145149..20780160hg38UCSC Ensembl
chr19:20255958..20962966hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38635012
hg19707009
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618290
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF486, ZNF626, ZNF737, ZNF826P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111753
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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