A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587167



Internal ID20960238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9194506..9194818hg38UCSC Ensembl
chr11:9216053..9216365hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219579
Samples
Known GenesDENND5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587167
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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