A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867169



Internal ID22642104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52559542..52564941hg38UCSC Ensembl
chr14:53026260..53031659hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459808
Samples
Known GenesGPR137C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867169
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