A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583149



Internal ID20956220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11533330..11553641hg38UCSC Ensembl
chr10:11575329..11595640hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3820312
hg1920312
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224672
Samples
Known GenesUSP6NL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583149
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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