A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543692



Internal ID20916938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240842221..240842885hg38UCSC Ensembl
chr1:241005521..241006185hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38665
hg19665
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250122
Samples
Known GenesRGS7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543692
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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