A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549764



Internal ID20922919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93562622..93563936hg38UCSC Ensembl
chr1:94028179..94029493hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg381315
hg191315
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252764
Samples
Known GenesBCAR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549764
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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