A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580095



Internal ID20953166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112449614..112449985hg38UCSC Ensembl
chr10:114209372..114209743hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224580
Samples
Known GenesVTI1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580095
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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