A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596773



Internal ID20969844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42060293..42060925hg38UCSC Ensembl
chr19:42564445..42565077hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246303
Samples
Known GenesGRIK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596773
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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