A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590065



Internal ID20963136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57544384..57545039hg38UCSC Ensembl
chr11:57311857..57312512hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229986
Samples
Known GenesSMTNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590065
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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