A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592341



Internal ID20965412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57706704..57707878hg38UCSC Ensembl
chr11:57474176..57475350hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381175
hg191175
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230893
Samples
Known GenesMED19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592341
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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