A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5626n100



Internal ID22791713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:34051421..34187597hg38UCSC Ensembl
chr5:34051526..34187702hg19UCSC Ensembl
chr5:34087283..34223459hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38136177
hg19136177
hg18136177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033827, nsv1021466
Samples
Known GenesC1QTNF3-AMACR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5626n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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