A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv168n100



Internal ID20151784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59538920..59592595hg38UCSC Ensembl
chr1:60004592..60058267hg19UCSC Ensembl
chr1:59777180..59830855hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3853676
hg1953676
hg1853676
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014113, nsv1008717, nsv1010742, nsv1010341, nsv1000043
Samples
Known GenesFGGY
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv168n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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