A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587939



Internal ID20961010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100159275..100160277hg38UCSC Ensembl
chr13:100811529..100812531hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg381003
hg191003
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225620
Samples
Known GenesPCCA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587939
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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