A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv581n100



Internal ID22786668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227008801..227084049hg38UCSC Ensembl
chr1:227196502..227271750hg19UCSC Ensembl
chr1:225263125..225338373hg18UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3875249
hg1975249
hg1875249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv997751, nsv1014423, nsv1012482
Samples
Known GenesCDC42BPA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv581n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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