A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596198



Internal ID20969269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9191684..9261386hg38UCSC Ensembl
chr19:9302360..9372062hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3869703
hg1969703
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246532
Samples
Known GenesOR7D4, OR7E24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596198
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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