A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542123



Internal ID20915389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168900592..168993392hg38UCSC Ensembl
chr1:168869830..168962630hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3892801
hg1992801
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248058
Samples
Known GenesLINC00970
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542123
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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