A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577590



Internal ID20950661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17426808..17429794hg38UCSC Ensembl
chr10:17468807..17471793hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg382987
hg192987
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234509
Samples
Known GenesST8SIA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577590
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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