A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548913



Internal ID20922091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8288628..8289043hg38UCSC Ensembl
chr1:8348688..8349103hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38416
hg19416
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253899
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548913
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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