A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584736



Internal ID20957807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46821422..46821912hg38UCSC Ensembl
chr11:46842973..46843463hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223331
Samples
Known GenesCKAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584736
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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