A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578136



Internal ID20951207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25703454..25703779hg38UCSC Ensembl
chr10:25992383..25992708hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223537
Samples
Known GenesLINC00836
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578136
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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