A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545189



Internal ID20918421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:90618067..90619972hg38UCSC Ensembl
chr1:91083624..91085529hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg381906
hg191906
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251988
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545189
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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