A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595999



Internal ID20969070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45672032..45673316hg38UCSC Ensembl
chr19:46175290..46176574hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg381285
hg191285
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245654
Samples
Known GenesGIPR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595999
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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