A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587331



Internal ID20960402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34685956..34835072hg38UCSC Ensembl
chr11:34707503..34856619hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38149117
hg19149117
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225988
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587331
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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