A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587288



Internal ID20960359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48199244..48206623hg38UCSC Ensembl
chr13:48773380..48780759hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg387380
hg197380
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587288
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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