A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv415n100



Internal ID20152031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152492368..152546721hg38UCSC Ensembl
chr1:152464844..152519197hg19UCSC Ensembl
chr1:150731468..150785821hg18UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3854354
hg1954354
hg1854354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012908, nsv1005553
Samples
Known GenesCRCT1, LCE5A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv415n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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