A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541332



Internal ID20914614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168878162..168878818hg38UCSC Ensembl
chr1:168847400..168848056hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38657
hg19657
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248057
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541332
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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