A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538195



Internal ID20911518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14452225..14453706hg38UCSC Ensembl
chr2:14592349..14593830hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg381482
hg191482
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254503
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538195
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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