A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578288



Internal ID20951359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59693870..59694446hg38UCSC Ensembl
chr10:61453628..61454204hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222385
Samples
Known GenesSLC16A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578288
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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