A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv239n137



Internal ID22812859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150821840..150821973hg38UCSC Ensembl
chr3:150539627..150539760hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv2806833, nsv2807956
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)dgv239n137
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