A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539350



Internal ID20912648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114698230..114698522hg38UCSC Ensembl
chr1:115240851..115241143hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249261
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539350
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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