A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585376



Internal ID20958447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:47856115..47857790hg38UCSC Ensembl
chr13:48430250..48431925hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg381676
hg191676
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228189
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585376
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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