A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552187



Internal ID20925315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87248189..87248463hg38UCSC Ensembl
chr3:87297339..87297613hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264055
Samples
Known GenesCHMP2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552187
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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