A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548798



Internal ID20921980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205724478..205725118hg38UCSC Ensembl
chr1:205693606..205694246hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249983
Samples
Known GenesNUCKS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548798
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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