A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv164n100



Internal ID22786251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:49558898..49954717hg38UCSC Ensembl
chr1:50024570..50420389hg19UCSC Ensembl
chr1:49797157..50192976hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38395820
hg19395820
hg18395820
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010476, nsv1003729
Samples
Known GenesAGBL4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv164n100
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