A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596938



Internal ID20970009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3139111..3139693hg38UCSC Ensembl
chr19:3139109..3139691hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245872
Samples
Known GenesGNA15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596938
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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