A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596096



Internal ID20969167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10266183..10266996hg38UCSC Ensembl
chr19:10376859..10377672hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38814
hg19814
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244974
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596096
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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