A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856757



Internal ID22631692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130113295..130120328hg38UCSC Ensembl
chr9:132875574..132882607hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg387034
hg197034
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511495
Samples
Known GenesGPR107
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856757
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer