A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554288



Internal ID20927391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:88934457..88935118hg38UCSC Ensembl
chr1:89400140..89400801hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251960
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554288
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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