A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586057



Internal ID20959128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28166012..28166711hg38UCSC Ensembl
chr10:28454941..28455640hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234707
Samples
Known GenesMPP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586057
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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