A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597216



Internal ID20970287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15722927..15842539hg38UCSC Ensembl
chr19:15833737..15953349hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38119613
hg19119613
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245801
Samples
Known GenesCYP4F24P, OR10H1, OR10H2, OR10H3, OR10H5, UCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597216
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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