A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597190



Internal ID20970261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20161822..20435068hg38UCSC Ensembl
chr19:20272631..20617874hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38273247
hg19345244
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246183
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF486, ZNF826P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597190
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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