A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545516



Internal ID20918746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156319200..156320324hg38UCSC Ensembl
chr1:156288991..156290115hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg381125
hg191125
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247156
Samples
Known GenesCCT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545516
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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