A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553172



Internal ID20926281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216085698..216086144hg38UCSC Ensembl
chr2:216950421..216950867hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259295
Samples
Known GenesTMEM169
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553172
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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