A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538139



Internal ID20911463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173801982..173802377hg38UCSC Ensembl
chr1:173771120..173771515hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248698
Samples
Known GenesCENPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538139
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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