A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv258n137



Internal ID22812878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2960880..2960958hg38UCSC Ensembl
chr4:2962607..2962685hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv2810234, nsv2810233
Samples
Known GenesNOP14
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)dgv258n137
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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