A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5198n100



Internal ID22791285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44948206..45004306hg38UCSC Ensembl
chr4:44950223..45006323hg19UCSC Ensembl
chr4:44644980..44701080hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3856101
hg1956101
hg1856101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004138, nsv1014721
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)dgv5198n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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