A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545612



Internal ID20918838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8058188..8058959hg38UCSC Ensembl
chr1:8118248..8119019hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253230
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545612
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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