A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599434



Internal ID20972505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38769860..38792818hg38UCSC Ensembl
chr19:39260500..39283458hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3822959
hg1922959
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3509n223
Supporting Variantsnssv18248376
Samples
Known GenesLGALS7, LGALS7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599434
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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