A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593202



Internal ID20966273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132440900..132444135hg38UCSC Ensembl
chr11:132310794..132314029hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383236
hg193236
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236474
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593202
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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