A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587008



Internal ID20960079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35278279..35278812hg38UCSC Ensembl
chr11:35299826..35300359hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229372
Samples
Known GenesSLC1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587008
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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