A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585864



Internal ID20958935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17767182..17767924hg38UCSC Ensembl
chr10:17809181..17809923hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38743
hg19743
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224560
Samples
Known GenesTMEM236
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585864
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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