A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590092



Internal ID20963163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13296565..13297457hg38UCSC Ensembl
chr10:13338565..13339457hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38893
hg19893
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234451
Samples
Known GenesPHYH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590092
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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