A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546641



Internal ID20919851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:197667092..197667534hg38UCSC Ensembl
chr1:197636222..197636664hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248195
Samples
Known GenesDENND1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546641
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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