A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2808572



Internal ID21253910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174704017..174705820hg38UCSC Ensembl
chr4:175625168..175626971hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg381804
hg191804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13687143
Samples
Known GenesGLRA3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2808572
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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