A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599707



Internal ID20972778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12725158..12726077hg38UCSC Ensembl
chr19:12835972..12836891hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38920
hg19920
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599707
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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