A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551790



Internal ID20924923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225910510..225942934hg38UCSC Ensembl
chr1:226098210..226130634hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg3832425
hg1932425
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249423
Samples
Known GenesLEFTY2, MIR6741, PYCR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551790
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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