A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577888



Internal ID20950959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27701559..27702068hg38UCSC Ensembl
chr13:28275696..28276205hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38510
hg19510
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232901
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577888
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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