A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597960



Internal ID20971031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14147922..14216560hg38UCSC Ensembl
chr21:15520243..15588881hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3868639
hg1968639
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254456
Samples
Known GenesLIPI, RBM11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597960
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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