A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596852



Internal ID20969923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16665116..16665864hg38UCSC Ensembl
chr19:16775927..16776675hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247560
Samples
Known GenesTMEM38A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596852
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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