A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592392



Internal ID20965463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83179292..83179910hg38UCSC Ensembl
chr11:82890334..82890952hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229528
Samples
Known GenesPCF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592392
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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