A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5215n100



Internal ID22791302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57169186..57237378hg38UCSC Ensembl
chr4:58035352..58103544hg19UCSC Ensembl
chr4:57730109..57798301hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3868193
hg1968193
hg1868193
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1008288, nsv1001702
Samples
Known GenesIGFBP7-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5215n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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