A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576985



Internal ID20950056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18670413..18671254hg38UCSC Ensembl
chr10:18959342..18960183hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235458
Samples
Known GenesARL5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576985
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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