A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv494n100



Internal ID22786581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:190028502..190087425hg38UCSC Ensembl
chr1:189997632..190056555hg19UCSC Ensembl
chr1:188264255..188323178hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3858924
hg1958924
hg1858924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014714, nsv1012448, nsv1005260, nsv1011414
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv494n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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