A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591560



Internal ID20964631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112806586..112807583hg38UCSC Ensembl
chr10:114566345..114567342hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38998
hg19998
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224306
Samples
Known GenesVTI1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591560
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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