A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584714



Internal ID20957785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118351920..118353525hg38UCSC Ensembl
chr11:118222635..118224240hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381606
hg191606
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228232
Samples
Known GenesCD3G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584714
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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