A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593511



Internal ID20966582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21101301..21108755hg38UCSC Ensembl
chr10:21390230..21397684hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg387455
hg197455
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219122
Samples
Known GenesNEBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593511
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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