A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588271



Internal ID20961342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:872302..1184832hg38UCSC Ensembl
chr10:918242..1230772hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38312531
hg19312531
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv598n223
Supporting Variantsnssv18233841
Samples
Known GenesADARB2, GTPBP4, IDI1, IDI2, IDI2-AS1, LARP4B, LINC00200, WDR37
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588271
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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