A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586700



Internal ID20959771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91998817..91999682hg38UCSC Ensembl
chr10:93758574..93759439hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38866
hg19866
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236260
Samples
Known GenesBTAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586700
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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