A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2808914



Internal ID21254252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187413757..187428815hg38UCSC Ensembl
chr3:187131545..187146603hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3815059
hg1915059
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13702117, nssv13707254
SamplesCHM13, CHM1
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2808914
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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