A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577635



Internal ID20950706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31343446..31343776hg38UCSC Ensembl
chr11:31364993..31365323hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234105
Samples
Known GenesDCDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577635
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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